All Webinars
2021
26 May 2021
10:00 - 14:00 EET, GMT +2
- Description
-
This online information session presents the practical guide How to submit CLH dossiers that will be published in May. This guide gives advice to dossier submitters on what to check before submitting the CLH dossier with the aim of reducing the number of dossiers for which an update is needed.
A survey will be launched after the event to collect feedback on the practical guide and information on the challenges the dossier submitters face in the preparation of CLH dossiers. The survey results will be discussed in a second information session, which will take place later in the autumn.
The event is particularly addressed to CLH dossier submitters of substances under the scope of REACH and active substances used in biocidal products and plant protection products.
To join the event, fill in this expression of interest form by 30 April. You can send questions to our experts in advance using the form or alternatively, ask us questions during the live Q&A session which will be open during the event. You will receive a confirmation e-mail with the login details closer to the event.
The information session will take place 26 May 2021 at 10:00 Helsinki Time (EEST, GMT +3)
If you have any questions, please contact classification (at) echa.europa.eu
- Date
- 26 May 2021
10:00 - 14:00 EET, GMT +2 - Agenda
- Participate
- Registration form
- More details
- Webinar page
15 April 2021
11:00 - 13:00 EET, GMT +2
- Description
-
ECHA has published its proposal to restrict the use of lead in ammunition for hunting and outdoor sports shooting as well as in fishing.
A six-month consultation was launched on 24 March 2021.
This information session introduces the REACH restriction process, describes the proposed restriction on lead in outdoor shooting and fishing and explains how to submit comments to the consultation.
No registration is required. Join the information session via our homepage on the day of the event at 11:00 EET.
You can send questions to our experts in advance using this form (until 17:00 EET 11 April). You may also ask us questions during in a live question and answer session on 15 April from 11:00 to 13:00 EET using this link or entering the event code #lead in Sli.do.com.
Further information:
- Have your say on proposed restriction of lead in outdoor shooting, hunting and fishing, 24 March 2021
- Towards sustainable outdoor shooting and fishing – ECHA proposes restrictions on lead use, 3 February 2021
- Hot topics: lead in shot, bullets and fishing weights
Agenda
Timing
Title
Speaker
11:00
Introduction to the information session and to the REACH restriction process
Mark Blainey
11:10
Details of the proposed restriction
Christiaan Logtmeijer
11:30
How to participate in the consultation
Peter Simpson
11:50
Concluding remarks and next steps
Mark Blainey
12:00-13:00
Question and answer session remains open
- Date
- 15 April 2021
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
31 March 2021
11:00 - 13:00 EET, GMT +2
- Description
- This webinar gives advice on how to prepare a poison centre notification.It is particularly helpful if:
- You are new to dossier preparation
- Your dossier is failing validation rules
- You need to make an update to your notification
The tips presented in this webinar were put together from real cases received by our support team.Questions and answers from the event.AgendaTiming
Title
Speaker
11:00
Introduction
Heidi Rasikari, ECHA
11:05
Best practice for preparing your notification
Heidi Rasikari, ECHA
11:25
Tips to understand and pass validation rules
Daniele Ape, ECHA
11:45
How to submit: pre and post submission
Claudia Rimondo, ECHA
12:05
Take home messages
Heidi Rasikari, ECHA
11:00 – 13:00
Webinar remains open for questions
Presentations
-
All slides in one [PDF] - Heidi Rasikari, Daniele Ape, Claudia Rimondo
- Date
- 31 March 2021
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
4 March 2021
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar focuses on new functionalities implemented in the latest version of REACH-IT (v3.9):
- New section on the co-registrants page with contact details of submitters of (robust) study summaries for data sharing purposes. The page also includes whether the (robust) study summaries have been submitted less or more than 12 years earlier
- New section on the joint submission page with information on ongoing and past dossier evaluations concerning any of the joint submission’s members
It also offers a summary of the main features of REACH-IT since 2020 and what to expect in 2021.
Questions and answers from the event.
Programme
Timing
Title
Speaker
11:00-11:05
Introduction
Eduardo López, ECHA
11:05-11:15
REACH-IT 2020/2021
Eduardo López, ECHA
11:15-11:40
Information on submitters and submission dates of (robust) study summaries on co-registrants page
Tuomas Aitasalo, ECHA
11:40-12:05
Dossier evaluation status in the joint submission
Reka Vataja, ECHA
Presentations
-
All slides in one [PDF] - Eduardo López, Tuomas Aitasalo, Reka Vataja
- Date
- 4 March 2021
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
26 January 2021
11:00 - 13:00 EET, GMT +2
- Description
-
French authorities propose to restrict PAHs, furans, dioxins, formaldehyde and PCBs in single-use baby diapers. The aim is to minimise health risks associated with wearing single-use diapers for children and infants under the age of three.
A consultation on the proposal was launched on 21 December and will end on 21 June 2021.
This info session gives an update on the proposed restriction, explains the specific questions posed in the consultation and clarifies how to submit comments.
Questions and answers from the event.
Programme
Time
Presentation
Speaker
11:00
Introduction to REACH restriction
Peter SIMPSON, ECHA
11:20
Proposed restriction
Céline DUBOIS & Karine FIORE, ANSES
11:40
Specific consultation questions
Sanna HENRICHSON, ECHA
11:55
How to submit information
Bastian ZEIGER, ECHA
12:00 – 13:00
Webinar remains open for questions
- Date
- 26 January 2021
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
20 January 2021
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar describes the new functionalities of Chesar 3.6, focusing on the implementation of a set of harmonised conditions of use for workers’ assessments. These conditions of use are the result of a mapping exercise with the owners of the most used workers’ assessment tools (i.e. ECETOC TRA, ART, Stoffenmanager, MEASE and EMKG-expo-tool).
Programme
Time
Presentation
Speaker
11:00
Introduction
Roberta Bernasconi
11:02
Chesar 3.6 what’s new
Roberta Bernasconi
11:20
Demo of Chesar 3.6
Eleni Tsitsiou
11:30
Concluding remarks
Roberta Bernasconi
11:00 – 13:00
Webinar open for questions
- Date
- 20 January 2021
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
2020
24 November 2020
12:30 - 13:30 EET, GMT+2
- Description
-
This webinar is dedicated to IUCLID users preparing the biocides submissions. It introduces a new dossier type for the Technical Equivalence and guides you through the format changes and improvement related to biocides, implemented in IUCLID 6.5 published on 28th of October 2020. The webinar provides also an update on the report generator for biocides as well as the plans for 2021. The webinar is an extension of IUCLID October 2020 release webinar on 11th November.
- Date
- 24 November 2020
12:30 - 13:30 EET, GMT+2 - Agenda
- More details
- Webinar page
19 November 2020
11:00 - 15:00 EET, GMT +2
- Description
-
This webinar helps you to get ready for preparing and submitting a SCIP notification.
You will get a demo of how to create and submit a notification and learn the tools that can be used to refer to information already successfully submitted to the SCIP database.
Date: 19 Nov 2020
Time: 11:00 – 15:00 Helsinki Time (EET, GMT+2)Agenda
Time Title Speaker 11:00 Introduction Clara Rueda 11:02 SCIP data preparation (‘Grouping’, ‘hierarchy’, recommendations) Telmo Vieira Prazeres 11:50 SCIP Tools Ferran Villar Garcia 12:10 Tools to refer to data already submitted to ECHA (‘Referencing’ and Simplified SCIP Notification) (DEMO) Tommy Hagg & Clara Rueda 13:08 Take home messages Clara Rueda 13:10-15:00 Webinar open for questions - Date
- 19 November 2020
11:00 - 15:00 EET, GMT +2 - Agenda
- More details
- Webinar page
11 November 2020
11:00 - 12:00 EEST
- Description
-
Watch our pre-recorded webinar where we present the scope of the latest IUCLID version (6.5) published on 28 October 2020.
IUCLID is updated twice a year. This October release reflects the latest EU, OECD and other format changes as well as an important milestone in the transition to the web user interface. During the webinar we will also provide some information about the update of IUCLID in the ECHA Cloud Services.
The web interface now contains almost all the features needed to perform advanced management of IUCLID data. We will introduce the latest features of the web interface such as:
- (advanced) Printing of dossiers
- (advanced) Import settings
- Navigation tree for datasets
- Dossiers search
- View of inbound references
- Bulk export and deletion of entities
- Questions and answers [PDF]
- Date
- 11 November 2020
11:00 - 12:00 EEST - Agenda
- More details
- Webinar page
4 November 2020
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar gives you the latest information and updates, helps you troubleshoot common IT problems, and presents the support material you need ahead of the upcoming compliance date.
We will cover new IT tool features resulting from changes in Annex VIII, and explain how to avoid common reasons for dossier failure. Our experts will be on standby to answer regulatory questions and to support you with any issues in preparing or submitting your notification.
The webinar will be published on our home page on 4 November at 11:00 Helsinki Time (EET, GMT +2).
No registration is required.
Agenda
Timing Title Speaker 11:00 Introduction (webinar open for questions) Heidi Rasikari 11:05 Annex VIII – 2nd amendment solutions Daniele Ape 11:15 PCN IT solution Claudia Rimondo 11:35 The latest in system to system Stefen Supanic 11:45 Validation tips for successful submissions Saara Sumiala 11:55 Guidance – what you need to know Pedro Roselló Vilarroig 12:05 Hot topics - support and practical advice Heidi Rasikari 12:15 - 13:00 Webinar open for questions - Webinar Q&A [PDF]
- Date
- 4 November 2020
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
29 October 2020
13:30 - 15:30 CET, GMT +1
- Description
-
Germany, the Netherlands, Norway, Sweden and Denmark are working on a REACH restriction proposal to limit the risks to the environment and human health from the manufacture and use of all per- and polyfluoroalkyl substances (PFAS). A call for evidence was held during the summer of 2020.
Join the webinar to learn about the REACH restriction process and status of the proposed PFAS restriction.
The webinar will be published on our home page on 29 October at 13:30 CET, GMT +1 together with instructions for joining a live Q&A session where experts from the 5 Member States will be answering your questions until 15:30. Join the Sli.do Q&A session or by going to slido.com and entering the event code: pfas2020
Five European states call for evidence on broad PFAS restriction - ECHA news release, 11 May 2020
Date: 29 October 2020
Time: 13:30–15:30 CET, GMT+1
Agenda
Timing Title Speaker 13:30 Introduction and Sli.do Q&A open for questions Peter Simpson, ECHA
Martijn Beekman, NL-CA13:36 Why is this restriction on PFAS needed? Jenny Ivarsson, SE-CA 13:49 REACH restriction process and status of the PFAS restriction Mandy Lokaj, DE-CA 14:07 Introduction to the panellists answering questions Martijn Beekman, NL-CA 14:14 Closing remarks Peter Simpson, ECHA 14:15 – 15:30 Sli.do Q&A open for questions Panel - Date
- 29 October 2020
13:30 - 15:30 CET, GMT +1 - Agenda
- More details
- Webinar page
15 October 2020
11:00 - 13:00 EEST, GMT +3
- Description
-
This webinar is for you if you work or plan to work with an application for product authorisation for a biocidal product family.
The aim of the webinar is to give you an overview of the state of play on biocidal product families in the EU. You will also hear about practical experience gained by a national authority and industry on the revised biocidal product family concept.
You can watch the webinar here or directly on our home page on the day of the event at 11:00 Helsinki time (EEST, GMT +3).
A live online Q&A session will take place when the webinar is published until 13:00 (GMT +3). You can join it here.
Agenda
Timing
Title
Speaker
11:00
Introduction
Chiara Pecorini, ECHA
11:05
State of play on biocidal product families
Vincent Delvaux, European Commission - DG Health and Food Safety
11:15
Experience from a national authority’s perspective
Thilo Walther, Federal Institute for Occupational Safety and Health, Germany (BAuA)
11:35
Experience from an industry perspective
Meredith Theelen, Ecolab
11:55
Conclusions
Chiara Pecorini, ECHA
11:00–13:00
Questions answered online
- Date
- 15 October 2020
11:00 - 13:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
24 September 2020
11:00 - 15:00 EEST, GMT +3
- Description
-
If you are planning to export hazardous chemicals outside the EU, you will most likely have to comply with the PIC Regulation. It covers for example industrial chemicals, pesticides, or biocides that are banned or severely restricted within the EU.
The webinar explains the scope and main requirements of the PIC Regulation. You will learn how to notify your exports and the conditions that require explicit consent from the importing countries. You will also learn how to report your imports and exports.
The webinar will be published on our home page on the day of the event at 11:00 Helsinki Time (EEST, GMT +3). No registration is required.
At the same time, we will open a live Q&A session through Slido where we will be answering your questions until 15:00 Helsinki Time.
You can join the Q&A directly or by going to slido.com and entering the event code: pic2020.
Agenda
Timing
Title
Speaker
11:00
Introduction
Salla GYNTHER
11:05
Scope and general overview of the PIC Regulation
Salla GYNTHER
11:20
Export notification and related procedures
Valeria YILMAZ
11:40
How to fill in an export notification
Ramona CIOATA
11:50
Annual reporting on PIC exports and imports
Ramona CIOATA
11:55
Concluding remarks
Ramona CIOATA
12:00–15:00
Questions
- Date
- 24 September 2020
11:00 - 15:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
9 June 2020
11:00 - 13:00 EEST, GMT + 3
- Description
-
Join this webinar to learn about the steps you need to take to make sure your company size has been declared correctly to avoid unnecessary fees.
What you can expect:
- Learn about the SME definition
- Learn how to assess your company size
- Examples of ownership structures and calculations
- Key messages and tips
- Date
- 9 June 2020
11:00 - 13:00 EEST, GMT + 3 - Agenda
- More details
- Webinar page
12 May 2020
10:00 - 11:00 EEST, GMT +3
- Description
-
Watch our pre-recorded webinar where we present the scope of the latest IUCLID version published on 29 of April.
IUCLID is updated twice a year. The October release introduces new format changes and the April release is dedicated to improvements and bug fixes.
The new version finalises the management of IUCLID inventories together with literature references, contacts and categories.
This webinar presents the new navigation tree for dossiers, advanced search for mixtures, substance and article datasets as well as bulk copying of documents.
The webinar will be published on our home page on the day of the event at 10:00 Helsinki Time (EEST, GMT +3). At the same time, we will open a live Q&A session through Slido where we will be answering your questions until 17:00 Helsinki Time.
You can join the Q&A directly or by going to slido.com and entering the event code: iuclidapril2020.
- Date
- 12 May 2020
10:00 - 11:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
23 April 2020
11:00 - 12:30 EEST, GMT +2
- Description
-
Germany has prepared a restriction proposal on Perfluorohexanoic acid (PFHxA) related substances. A 6 month consultation started on 25 March.
PFHxAs are very versatile and have been used in various sectors such as clothing, polymers and fire extinguishing agents. Their persistent and mobile properties make the control of emissions and exposure difficult, and they can cause adverse effects to our health and the environment.
This info session gives an update on the proposed restriction, clarifies its scope and how to prepare and submit comments in the consultation.
- Date
- 23 April 2020
11:00 - 12:30 EEST, GMT +2 - Agenda
- More details
- Webinar page
17 March 2020
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar describes the state of play of the SCIP database, following the launch of its prototype in February. Join our webinar for a demo of how to create and submit a SCIP notification and use the opportunity to ask questions from our experts.
SCIP is a database for information on substances of concern in articles as such or in complex objects (products) established under the Waste Framework Directive.
Companies supplying articles containing substances of very high concern (SVHCs) on the Candidate List in a concentration above 0.1% weight by weight (w/w) on the EU market have to submit information on these articles to ECHA, as of 5 January 2021.
- Date
- 17 March 2020
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
4 March 2020
11:00 - 13:00 EET, GMT +2
- Description
-
EUCLEF will be launched in March. It is a new service from ECHA that puts 40 pieces of EU chemicals legislation at your fingertips, enabling you to find out how your substances are regulated in the EU and what legal obligations you have.
Join our webinar to get a sneak preview of how the finder works and ask questions from our experts.
- Date
- 4 March 2020
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
24 February 2020
12:00 - 14:00 EET, GMT +2
- Description
-
Updated REACH information requirements for nanoforms of substances apply as of 1 January 2020. Beyond this date, companies must have a registration compliant with these requirements to manufacture or import nanoforms of substances that fall within the scope of REACH.
Join our webinar to hear about the registrations received so far, key lessons learnt and best practices. Use the opportunity to ask questions on how to prepare registration dossiers for your nanoforms and get practical advice from our experts for successfully submitting your registration.
Agenda
Timing
Title
12:00
Introduction and general observations on nanoform registrations
12:10
Practical advice based on received registrations
12:45
Conclusions
12:50 – 14:00
Webinar open for questions
Further information
- Companies need to provide more data on nanoforms, News release 24 February 2020
- Watch our previous webinar: Getting ready for revised REACH information requirements for nanomaterials
- Date
- 24 February 2020
12:00 - 14:00 EET, GMT +2 - Agenda
- More details
- Webinar page
12 February 2020
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar gives you an update on the latest and upcoming developments for notifying your hazardous mixtures to poison centres. These include changes to Annex VIII and improvements to our IT tools and available support.
It also gives you the chance to ask questions from our experts on the regulatory and IT aspects of the notification process.
Agenda
Timing
Title
11:00
Welcome and introduction, Heidi Rasikari - ECHA
11:10
Regulatory update, Daniele Ape - ECHA
11:30
PCN IT tools update, Claudia Rimondo - ECHA
11:50
Guidance and support update, Heidi Rasikari - ECHA
12:00 – 13:00
Time reserved for Q&A
- Date
- 12 February 2020
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
30 January 2020
11:00 - 12:30 EET, GMT +2
- Description
-
The French Agency for Food, Environmental and Occupational Health & Safety (ANSES) announced its intention to propose a restriction of PAHs, furans, dioxins, PCBs and formaldehyde in single-use nappies for infants and children.
We will host a call for evidence to support the preparation of the proposal. The call for evidence starts in January 2020 and closes on 31 March 2020.
This information session is intended to clarify the scope of ANSES’ investigation and answer your questions related to the call for evidence. It is open for all, and will be most useful for those planning to provide information for the preparation of the restriction proposal.
Media are invited to send their enquiries to press [at] echa.europa.eu.
Agenda
Time
Title
Speaker
11:00
Introduction to the session and its purpose
Peter Simpson, ECHA
11:10
Scope of the investigation
Karine Fiore, ANSES
11.50
Q&A
Karine Fiore and Céline Dubois, ANSES
Moderator: Peter Simpson, ECHA
12:25
Concluding remarks and next steps
Peter Simpson, ECHA
12:30
Webinar ends
- Date
- 30 January 2020
11:00 - 12:30 EET, GMT +2 - Agenda
- More details
- Webinar page
29 January 2020
11:00 - 13:00 EET, GMT +2
- Description
-
To help companies facing difficulties due to the COVID-19 pandemic, the completeness checks of chemical safety reports will now only start in October 2020. The remaining changes to the completeness check will take effect on submissions as of 1 May 2020, as previously communicated.
The completeness check includes more explicit rules to ensure that registrants address information requirements for key hazard endpoints and strengthened checks for reporting the substance life cycle. The completeness check will also be extended to cover an area of the registration that was previously not verified – the chemical safety report.
Join our webinar to find out about the upcoming changes and get a head start in preparing your registration for the revised checks.
Use the opportunity to ask questions from our experts.
Agenda
11:00
Introduction
Robert LUCAS, ECHA
11:10
Revised completeness check of Annex VII-XI information requirements
Ella LAAKKONEN, ECHA
11:20
Completeness check of the chemical safety report: what is covered
Valerie LASSEIGNE-PHRAKONKHAM, ECHA
11:30
Practical examples: ensuring a complete chemical safety report
Soile NIEMI, ECHA
Andreas AHRENS, ECHA
11:55
Conclusions
Robert LUCAS, ECHA
- Date
- 29 January 2020
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
2019
26 November 2019
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar gives you the latest information about ECHA’s and industry’s action plans for addressing the lack of compliance of REACH registration dossiers. The webinar is an opportunity for you to learn about the overall context and impact of upcoming changes and how you can prepare.
You will have the chance to ask questions from our experts.
Agenda
Timing
Title
Speaker
11:00
Introduction
Christel Musset, ECHA
11:20
Joint action plan to tackle REACH compliance
Laurence Hoffstadt, ECHA
11.40
Cefic action plan for review and improvement of registration dossiers
Mariana Fernandes de Barros, Cefic
12:00
Conclusions
Christel Musset, ECHA
12:10 – 13:00
Webinar open for questions
- Date
- 26 November 2019
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
12 November 2019
11:00 - 13:30 EET, GMT +2
- Description
-
Updated REACH Annexes for the nanoforms of substances begin to apply as of 1 January 2020. The updated Annexes introduce new concepts: nanoform and a set of similar nanoforms. The updated REACH Annex VI also defines specific characterisation parameters for the nanoforms of substances.
The first part of this webinar explains what a nanoform is and how to build a set of similar nanoforms. It also explains how to fulfil data requirements for the characterisation of nanoforms. The second part introduces new IUCLID fields for reporting the characterisation parameters of nanoforms and gives some practical examples on how to use the different fields. You will also have the chance to ask questions from our experts.
- Date
- 12 November 2019
11:00 - 13:30 EET, GMT +2 - Agenda
- More details
- Webinar page
8 November 2019
11:00 - 12:00 EET, GMT +2
- Description
-
A new IUCLID will be available on 30 October.
Version 6.4.0 takes into account changes to the REACH Regulation, including new data fields for reporting nanoforms as well as the latest amendments (ATPs) to the CLP Regulation.
It also contains new features for the upcoming database on substances of very high concern in articles (SCIP) and supports the needs of several regulatory authorities, in particular the European Food Safety Authority (EFSA), and the authorities managing chemicals in Australia and New Zealand.
The web user interface has also been improved with direct navigation to referenced documents in dossiers, advanced printing options and a more compact document view.
Join the webinar to learn more about the new features and use the opportunity to ask questions from our experts.
- Date
- 8 November 2019
11:00 - 12:00 EET, GMT +2 - Agenda
- More details
- Webinar page
28 October 2019
16:00 - 18:00 EET, GMT +2
- Description
-
This webinar introduces how the GreenScreen methodology and tool enable you to compare substances on multiple hazard endpoints and rank them according to four benchmarks. You will hear examples of how companies and authorities use it to find safer alternatives to substances of concern.
You will also have the chance to ask questions from the presenters.
Agenda
Timing
Title
Speaker
16:00
Introduction
Adam Elwan, ECHA
16:10 – 16.35
Introduction to GreenScreen for Safer Chemicals
Shari Franjevic, Clean Production Action
16.35 – 16:50
GreenScreen in Government – the case of Washington State Department of Ecology
Brian Penttila, Washington State Department of Ecology
16:50 – 17:05
The business case for alternatives assessment – How HP uses GreenScreen
Cory Robertson, Hewlett Packard
17:05 – 17:25
Applying GreenScreen in the European context
Paul Ashford, Anthesis Group
17:25 – 17:35
Conclusions
Adam Elwan, ECHA
17:35 – 18:15
Webinar open for questions
- Date
- 28 October 2019
16:00 - 18:00 EET, GMT +2 - Agenda
- More details
- Webinar page
17 October 2019
11:00 - 13:00 EET, GMT +2
- Description
-
EUSES is a tool that enables you to carry out chemical risk assessments.
Join our webinar to learn about the new features of EUSES version 2.2.0. We will cover the new and updated environmental emission scenarios for biocides, the new emission pathway of direct releases to the environment and the new version of the SimpleTreat model (4.0).
If you are a company working on environmental risk assessment of biocides, this webinar will be particularly useful for you.
You will have the chance to ask questions from our expert panel.
Agenda
Timing
Title
Speaker
11:00
Introduction
Heike SCHIMMELPFENNIG, ECHA
11:10
Live demo: how to use EUSES 2.2.0
Eugénia NOGUEIRO, ECHA
11.50
Conclusions
Heike SCHIMMELPFENNIG, ECHA
12:00 – 13:00
Q&A
Heike SCHIMMELPFENNIG, Eugénia NOGUEIRO, and Adriana LIPKOVA - ECHA
- Date
- 17 October 2019
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
10 October 2019
11:00 - 12:30 EET, GMT +2
- Description
-
As a follow-up to the proposed restriction on the use of lead in shot in wetlands, ECHA has been requested by the commission to prepare a restriction proposal on the placing on the market and use of lead in ammunition (shot and bullets) and fishing tackle.
This information session is intended to clarify the scope of ECHA’s investigation and answer your questions related to the call for evidence.
The session is intended for stakeholders planning to provide relevant information for the preparation of the restriction proposal. The call for evidence is open until 16 December 2019.
The session is open to all. The maximum capacity is 1 000 participants.
Media are invited to send their enquiries to press [at] echa.europa.eu.
Agenda
Timing
Title
Speaker
11:00
Introduction
Mark Blainey, ECHA
11:05
Presentation 1: Scope of the investigation
Christiaan Logtmeijer, ECHA
11:25
Q&A
Christiaan Logtmeijer, Peter Simpson and Ida Lehtimäki - ECHA
Moderator: Mark Blainey, ECHA
12:25
Concluding remarks and next steps
Mark Blainey, ECHA
12:30
Webinar ends
Further information: - Date
- 10 October 2019
11:00 - 12:30 EET, GMT +2 - Agenda
- More details
- Webinar page
15 May 2019
11:00 - 12:00 EEST
- Description
-
This webinar will introduce you to the latest IUCLID web interface improvements and functionalities for biocides submissions. The webinar presents features such as the creation and navigation of a BPR dossier, the comparison tool, and the report generator.
- Date
- 15 May 2019
11:00 - 12:00 EEST - Agenda
- More details
- Webinar page
29 April 2019
13:00 - 14:30 EEST
- Description
-
A new service release of IUCLID 6 will feature an enhanced and improved web user interface, including the management of reference substances, an improved comparison and validation report, clearer navigation through your dataset’s information, the full report generator, as well as advanced dossier creation and import settings. It also includes a guided dossier approach for Poison Centre Notification (PCN) which allows you to prepare notifications for hazardous mixtures. The guided dossier approach provides a simplified, task-based, approach to dossier creation.
Join this webinar to find out about the changes and use the opportunity to ask questions from our experts.
- Date
- 29 April 2019
13:00 - 14:30 EEST - Agenda
- More details
- Webinar page
3 April 2019
11:00 - 13:00 EET, GMT +2
- Description
-
This online information session will provide an update on the proposed restriction on the placing on the market of intentionally-added microplastics, which was submitted to ECHA’s scientific committees on 11 January 2019. Following the required conformity check, a 6 month public consultation on the proposal started on 20 March. This webinar will introduce the detail of the proposal and clarify the objectives of the public consultation.
The session will also provide an opportunity for our panel of experts to answer any questions on the proposal and how to prepare and submit any comments in the consultation.
Agenda
Timing
Title
Speaker
11:00
Introduction to webinar and its purpose
Mark Blainey
11:10 – 11.30
Presentation 1: Scope of the proposed restriction
Peter Simpson
11.30 – 12.00
Q&A on the scope of the proposed restriction
Peter Simpson, Pertti Elo and Anu Kapanen
Moderator: Mark Blainey
12:00 – 12:10 Break 12:10 – 12:20
Presentation 2: Participating in the public consultation
Evgenia Stoyanova
12:20 – 12:50
Q&A on the public consultation
Evgenia Stoyanova, Peter Simpson and Sanna Henrichson.
Moderator: Mark Blainey
12:50 – 13:00
Concluding remarks and next steps
Mark Blainey
- Date
- 3 April 2019
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
2018
11 December 2018
11:00 - 12:00 EET, GMT +2
- Description
-
This online information session gives you the latest information for getting prepared with your notifications to poison centres. We will explain what you need to do step by step to prepare and submit your notifications and also give you the chance to ask questions from our live panel of experts.
- Date
- 11 December 2018
11:00 - 12:00 EET, GMT +2 - Agenda
- More details
- Webinar page
31 October 2018
11:00 - 13:00 EET, GMT +2
- Description
-
A new major version of IUCLID will be made available at the end of October.
IUCLID 6.3 will feature, in addition to the interface you already know, a completely new user interface that runs in a standard web browser, with no need to install any other software. The new interface provides a more streamlined user-experience, whilst still containing the basic IUCLID features needed to prepare a REACH, CLP or BPR dossier.
It also brings changes to the IUCLID format including the latest OECD harmonised templates, specific elements for microorganism datasets and support for European poison centre notifications.
Join this webinar to find out about the changes and use the opportunity to ask questions from our experts.
Recording
- Date
- 31 October 2018
11:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
19 September 2018
11:00 - 13:00 EEST, GMT +3
- Description
-
As of 1 January 2019, we will start checking the compliance of all relevant dossiers for a given substance and will address decisions to all registrants with non-compliant dossiers. This is a change from the current practice of addressing mainly lead registrants. Similarly, we will address our decisions on testing proposals to those registrants who plan to use a proposed test to fulfill their information requirement.
This information session presented the changes and gave participants the chance to ask questions.
- Date
- 19 September 2018
11:00 - 13:00 EEST, GMT +3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
19 June 2018
11:00 - 13:00 EEST, GMT +3
- Description
-
The criteria for identifying endocrine disrupting properties for biocides apply from 7 June. This webinar explains the scope of the criteria and how authorities are using them to assess biocides. We also go through the main advice in the newly published guidance on endocrine disruptors.
- Date
- 19 June 2018
11:00 - 13:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
17 May 2018
11:00 - 13:00 EEST, GMT +3
- Description
-
Are you preparing to register for the 31 May 2018 REACH deadline? Do you have questions about preparing and submitting your registration dossier? Join our last minute advice, questions and answers session, where you can ask our expert panel about all aspects of registration, from knowing your portfolio and finding your co-registrants to preparing and submitting your registration dossier.
- Date
- 17 May 2018
11:00 - 13:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
26 April 2018
11:00 - 12:00 EEST, GMT +3
- Description
-
This webinar explains what the unique formula identifier (UFI) is and how it can be used. It also describes available tools and support for generating and using the UFI for hazardous and non-hazardous mixtures. We will give you practical examples of different ways for using the UFI and you have the chance to ask questions from our experts.
Agenda
Timing
Title
Speaker
11:00
Introduction
Heidi Rasikari, ECHA
11:05
What is a UFI?
Heidi Rasikari, ECHA
11:20
Creating and using the UFI
Daniel Sompolski, ECHA
11:40
Managing your UFI
Daniele Ape, ECHA
11:55
Conclusions
Daniele Ape, ECHA
- Date
- 26 April 2018
11:00 - 12:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
19 April 2018
11:00 - 12:30 EEST, GMT +3
- Description
-
Are you preparing to register for the 31 May 2018 REACH deadline? Do you have questions about preparing and submitting your registration dossier? Join our questions and answers session where you can ask our expert panel about all aspects of registration, from knowing your portfolio and finding your co-registrants to preparing and submitting your registration dossier.
- Date
- 19 April 2018
11:00 - 12:30 EEST, GMT +3 - Agenda
- More details
- Webinar page
18 April 2018
15:00 - 16:30
- Description
-
Successful substitution requires tools to help you find the most suitable methods for framing your substitution project and analysing available alternatives. They can also support you in finding relevant substance data and partners. This webinar will give you an overview of some of the available tools to help you make the transition to safer chemicals.
ECHA strategy to promote substitution to safer chemicals
More about substitution on the ECHA website
Agenda
Timing
Title
Speaker
15:00
Introduction and ECHA's strategy to support substitution to safer chemicals
Adam Elwan, ECHA
15:15
Landscape of methods and tools to support transition to safer chemicals: lessons learned
Joel Tickner & Molly Jacobs, University of Massachusetts, Lowell
15:30
Demonstration of the OECD Substitution and Alternatives Assessment Toolbox
Emily Connor, Abt Associates
15:45
ChemSec Marketplace: dating site for safer alternatives
Jerker Ligthart, ChemSec
16:00
Using ECHA's data to support substitution
Eoin Brennan, ECHA
16:15
Conclusions
Adam Elwan, ECHA
- Date
- 18 April 2018
15:00 - 16:30 - Agenda
- More details
- Webinar page
15 March 2018
11:00 - 12:00 EET, GMT +2
- Description
-
This webinar is relevant to any company preparing a REACH registration dossier. It focuses on manual checks performed by ECHA as part of the completeness check and the most common failures. You will receive advice on how to avoid these failures to prepare a registration dossier that can be successfully submitted. You can send your questions to our experts throughout the webinar. Note that we cannot answer questions on specific submissions - you can send those to us using our contact form.
Timing Title Speaker 11:00 Introduction Sandra Murras, ECHA 11:05 Completeness check process Mariia Aleksanian, ECHA 11:15 Validation assistant Mariia Aleksanian, ECHA 11:25 Manual checks and most common failures Ella Laakkonen, ECHA 11:45 Frequently asked questions and support Laura Lee, ECHA 11:55 Conclusions Sandra Murras, ECHA 12:00-13:00 Time reserved for answering unanswered questions - Date
- 15 March 2018
11:00 - 12:00 EET, GMT +2 - Agenda
- More details
- Webinar page
12 March 2018
11:00 - 12:30 EET, GMT +2
- Description
-
This information session is intended to clarify the scope and answer your questions related to the call for evidence for the possible restriction on intentionally added microplastics in products of any kind.
The session is targeted at stakeholders planning to provide relevant information for the preparation of the restriction proposal. The call for evidence is open until 11 May 2018.
The session is open-to-all. The maximum capacity is 1 000 participants.
The most frequently asked questions and their answers will be published on this page after the event.
Media are invited to send their enquiries to press [at] echa.europa.eu.
Watch the recording:
Further information
- Date
- 12 March 2018
11:00 - 12:30 EET, GMT +2 - Agenda
- More details
- Webinar page
8 March 2018
11:00 - 12:00 EET, GMT +2
- Description
-
Join this webinar to get last minute advice on how to successfully submit your REACH registration dossier and take the opportunity to ask questions directly from our experts.
Agenda
Timing
Title
Speaker
11:00
1. Introduction
Alexis Quintana-Sáinz
11:05
2. Before submitting your dossier
István Mák
11:25
3. Data requirements
Kristina Laitinen
11:35
4. Get the correct invoice
Anita Etholen
11:45
5. Protect your confidential data
Éva Mák
11:55
6. Take home messages
Alexis Quintana-Sáinz
12:00
Time reserved for answering remaining questions
- Date
- 8 March 2018
11:00 - 12:00 EET, GMT +2 - Agenda
- More details
- Webinar page
7 February 2018
12:00 - 13:00 EET, GMT +2
- Description
-
The webinar covers a feature for SMEs, launched in December 2017 that provides an alternative method for preparing IUCLID dossiers using IUCLID Cloud. This feature, named ‘Guided dossier preparation for REACH 2018’, presents an SME with a series of well-defined tasks to complete based on the type of dossier they intend to submit to us. The guided approach includes task-specific help and links to relevant guidance documents and texts.
- Date
- 7 February 2018
12:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
1 February 2018
11:00 - 12:00
- Description
-
In January every year, a number of substances are marked for manual screening by Member States. The selection aims to identify substances that may have hazardous properties and the potential for exposure to us or the environment.
This webinar explains the screening process, its timelines, and the criteria for shortlisting. It also explains how registrants can influence the manual screening process by updating their dossiers and how they can get more information on common screening.
The webinar also gives advice on how registrants should react to informative letters sent by us to all registrants of shortlisted substances.
Programme
Timing Title Speaker 11:00 Introduction Hannu Braunschweiler, ECHA 11:10 General introduction to common screening Palmi Atlason, ECHA 11:30 Grouping of substances in screening Giovanni Bernasconi, ECHA 11:45 2018 shortlisting letter campaign: scope and expected outcome Chrystele Tissier, ECHA 12:00-13:00 Time reserver for answering unanswered questions - Date
- 1 February 2018
11:00 - 12:00 - Agenda
- More details
- Webinar page
2017
30 November 2017
11:00 - 13:00 EET, GMT +2
- Description
-
This webinar explains the support documentation available for registrants that cover nanoforms in their registration dossier. The main focus is on the registration and read-across of nanoforms, but the main updates for information requirements for human health and the environment will also be covered.
Note: some parts of this webinar are outdated. Specifically related to: registration, characterisation and substance identification. For the most up-to-date advice, refer to the latest webinars and guidance. - Date
- 30 November 2017
11:00 - 13:00 EET, GMT +2 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
15 November 2017
12:00 - 13:00 EET, GMT +2
- Description
-
This webinar is intended for IUCLID 6 users. It presents the content of the IUCLID 6 update published on 15 November 2017. It builds on feedback received from users after the IUCLID 6 releases and addresses the most frequently asked questions and reported issues.
Programme:
- Welcome and introduction
- Information on IUCLID version 6.2
- Compatibility between IUCLID versions
- Fee calculator
- Update on ECHA Cloud Services and IUCLID Cloud
- Questions and Answers
- Date
- 15 November 2017
12:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
2 November 2017
11:00 - 12:00 EET
- Description
-
This webinar explains the communication and notification obligations that EU importers, producers and suppliers of articles may have when their articles contain Candidate List substances. Particular focus is given to complex objects made up of more than one article.
- Date
- 2 November 2017
11:00 - 12:00 EET - Agenda
- Download agenda [PDF]
- More details
- Webinar page
10 October 2017
11:00 - 12:00 EEST, GMT +3
- Description
-
This webinar gives an overview of the harmonisation of information submitted for hazardous mixtures to poison centres in the European Union as of 2020. It is open to all interested parties but particularly relevant for industry and authorities. Participants will get recommendations on how to prepare for new notifications and have the chance to ask questions from our expert panel.
- Date
- 10 October 2017
11:00 - 12:00 EEST, GMT +3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
3 October 2017
11:00 - 12:00 EEST, GMT +3
- Description
-
This webinar gives an overview of the harmonisation of information submitted for hazardous mixtures to poison centres in the European Union as of 2020. It is open to all interested parties but particularly relevant for industry and authorities. Participants will get recommendations on how to prepare for new notifications and have the chance to ask questions from our expert panel.
- Date
- 3 October 2017
11:00 - 12:00 EEST, GMT +3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
20 September 2017
11:00 - 12:00 EEST, GMT + 3
- Description
-
The webinar is intended for industry to receive an introduction on:
- ECHA Cloud services and the IUCLID Cloud for SMEs
- How to subscribe to the cloud and manage your account
- How to use the cloud and create a dossier
You will have the chance to ask questions from our expert panel.
- Date
- 20 September 2017
11:00 - 12:00 EEST, GMT + 3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
19 May 2017
11:00 - 15:00 EEST, GMT +3
- Description
-
Welcome to the REACH 2018 Spring School!
During this intensive week, we will be broadcasting all the REACH 2018 phase webinars again with the possibility to ask questions from our experts. In addition, a new webinar: Getting your chemical safety assessment done will take place live from Helsinki on Day 3 of the Spring School, Wednesday 17 May.
Here you can register for the fifth day taking place on Friday 19 May.
During the day, we will broadcast the sixth REACH 2018 webinar and you will have the chance to ask questions.
Agenda:
11:00 - 12:00 Re-run webinar: Submit your registration dossier
12:00 - 15:00 Extended question and answer session on all REACH 2018 phases
- Date
- 19 May 2017
11:00 - 15:00 EEST, GMT +3 - Agenda
- More details
- Webinar page
18 May 2017
11:00 - 13:30 EEST, GMT +3
- Description
-
Welcome to the REACH 2018 Spring School!
During this intensive week, we will be broadcasting all the REACH 2018 phase webinars again with the possibility to ask questions from our experts. In addition, a new webinar: Getting your chemical safety assessment done will take place live from Helsinki on Day 3 of the Spring School, Wednesday 17 May.
Here you can register for the fourth day taking place on Thursday 18 May.
During the day, we will broadcast the fifth REACH 2018 webinar and you will have the chance to ask questions.
Agenda:
11:00 - 12:30 Re-run webinar: Prepare your registration as a IUCLID dossier
12:30 - 13:30 Extended question and answer session
- Date
- 18 May 2017
11:00 - 13:30 EEST, GMT +3 - Agenda
- More details
- Webinar page
17 May 2017
11:00 - 13:00 EEST, GMT +3
- Description
-
Welcome to the REACH 2018 Spring School!
During this intensive week, we will be broadcasting all the REACH 2018 phase webinars again with the possibility to ask questions from our experts. In addition, a new webinar: Getting your chemical safety assessment done will take place live from Helsinki on Day 3 of the Spring School, Wednesday 17 May.
Here you can register for the third day taking place on Wednesday 17 May.
During the day, we will broadcast a new webinar on getting your chemical safety assessment done and you will have the chance to ask questions.
- Date
- 17 May 2017
11:00 - 13:00 EEST, GMT +3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
16 May 2017
11:00 - 15:30 EEST, GMT +3
- Description
-
Welcome to the REACH 2018 Spring School!
During this intensive week, we will be broadcasting all the REACH 2018 phase webinars again with the possibility to ask questions from our experts. In addition, a new webinar: Getting your chemical safety assessment done will take place live from Helsinki on Day 3 of the Spring School, Wednesday 17 May.
Here you can register for the second day taking place on Tuesday 16 May.
During the day, we will broadcast the third and fourth REACH 2018 webinars and you will have the chance to ask questions.
Agenda:
11:00 - 12:10 Re-run webinar: Get organised with your co-registrants
12:10 - 12:40 Break
12:40 - 14:00 Re-run webinar: Assess hazards and risks
14:00 - 15:30 Extended question and answer session
- Date
- 16 May 2017
11:00 - 15:30 EEST, GMT +3 - Agenda
- More details
- Webinar page
15 May 2017
11:00 - 15:30 EEST, GMT +3
- Description
-
Welcome to the REACH 2018 Spring School!
During this intensive week, we will be broadcasting all the REACH 2018 phase webinars again with the possibility to ask questions from our experts. In addition, a new webinar: Getting your chemical safety assessment done will take place live from Helsinki on Day 3 of the Spring School, Wednesday 17 May.
Here you can register for the first day taking place on Monday 15 May.
During the day, we will broadcast the first two REACH 2018 webinars and you will have the chance to ask questions.
Agenda:
11:00 - 12:00 Re-run webinar: Know your portfolio and start preparing now
12:00 - 12:30 Break
12:30 - 13:30 Re-run webinar: Find your co-registrants and prepare to work together
13:30 - 15:30 Extended question and answer session
- Date
- 15 May 2017
11:00 - 15:30 EEST, GMT +3 - Agenda
- More details
- Webinar page
4 May 2017
12:00 - 13:00 EEST, GMT +2
- Description
-
This webinar is intended for users of IUCLID 6 and introduces the content of the IUCLID 6 update published on 28th of April 2017. It also addresses most frequently asked questions and reported issues.
Programme:
- Welcome and introduction
- Information on IUCLID 6 version 1.3:
- Improvements and fixes for known issues
- New features (PNEC generator, dossier header re-use)
- Advanced features of the report generator
- Questions and Answers
- Date
- 4 May 2017
12:00 - 13:00 EEST, GMT +2 - Agenda
- More details
- Webinar page
20 April 2017
11:00 - 12:00 EEST, GMT +3
- Description
-
This webinar is relevant for any company preparing a REACH registration dossier.
It focusses on experience gained since the revised completeness check was introduced in June 2016. You will also get valuable insight into the manual checks performed by ECHA staff as part of the completeness check.
During the webinar, you can send your questions to our experts. Note that we cannot answer questions on specific submissions - you can send those to us using our contact form.
- Date
- 20 April 2017
11:00 - 12:00 EEST, GMT +3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
30 March 2017
11:00 - 13:00 EEST, GMT +3
- Description
-
This webinar is of interest for downstream users and downstream user sector organisations who want to optimise the communication of safe use information in the supply chain.
Participants will learn about the sector use map concept, its benefits, and its implementation.
Downstream users need to ensure they meet the conditions described in the exposure scenarios they receive. It is key that these exposure scenarios reflect the conditions of use in place, where those can be demonstrated to be safe. Exposure scenarios are generated by registrants. Therefore downstream users need to communicate to registrants how their substances are used. Sector use maps are an efficient way of communicating such information to registrants.
Sector use maps avoid the need for bilateral contacts between downstream users and registrants and ensure that downstream users receive realistic and harmonised exposure scenarios, making them easier to process.
Summary of panel Q&A
- Download [PDF]
- Date
- 30 March 2017
11:00 - 13:00 EEST, GMT +3 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
23 February 2017
11:00 - 12:15 EET, GMT+2
- Description
-
The webinar presents how H&M and a group of Italian SMEs from the Prato district have organised themselves to replace harmful chemicals from their supply chains. Greenpeace will also present their Detox campaign, the International Chemical Secretariat (ChemSec) will give an overview of their available tools to help companies substitute and the European Textile and Apparel Association (EURATEX) will present their activities in replacing harmful chemicals.
- Date
- 23 February 2017
11:00 - 12:15 EET, GMT+2 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
14 February 2017
11:00 - 13:00 EET
- Description
-
ECHA and Member State Competent Authorities are now in the fourth year of common screening. In late January every year, a number of substances are marked for manual screening by Member States. The selection is based on a set of algorithms to identify substances that may have hazardous properties and have the potential for exposure to humans or the environment.
This webinar explains the screening process, its timelines, and the criteria for short listing. It also explains how registrants can influence the manual screening process by updating their dossiers and how they can obtain more information on common screening.
The webinar also gives advice on how registrants should react to the informative letters sent by ECHA to all registrants of shortlisted substances.
- Date
- 14 February 2017
11:00 - 13:00 EET - Agenda
- Download agenda [PDF]
- More details
- Webinar page
2 February 2017
12:00 - 13:00 EET, GMT +2
- Description
-
This webinar is intended for users of IUCLID 6. It presents the content of the IUCLID 6 update published on 31st of January 2017. It builds on feedback received from users after previous IUCLID 6 releases and addresses the most frequently asked questions and reported issues.
Programme:
- Welcome and introduction
- Information on IUCLID 6 version 1.2
- Fixes for known issues
- New features (DNEL generator, hyperlinks, IUCLID Public API)
- Advanced feature of the Report generator
- Tips for registrants
- Questions and Answers
- Date
- 2 February 2017
12:00 - 13:00 EET, GMT +2 - Agenda
- More details
- Webinar page
2016
30 November 2016
11:00 - 12:00 EET, GMT +2
- Description
-
So, your IUCLID dossier is ready, what now? This webinar will show you how easy it is to navigate around REACH-IT and submit your dossier to ECHA. We will also explain and guide you through some of the most important new features of REACH-IT such as identifying the ‘tasks’ assigned to you and how to act on them, using the joint submission page, as well as how to manage and change your company information.
- Date
- 30 November 2016
11:00 - 12:00 EET, GMT +2 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
4 October 2016
11:00 - 12:00 EET (GMT +2)
- Description
-
This is the fifth webinar in a series focusing on practical advice to successfully register by the REACH 2018 registration deadline of 31 May 2018.
If you are registering a substance for the first time and want to know how to use IUCLID to create a registration dossier, then this webinar is for you.
We will guide you through the different steps that are needed to successfully create a complete registration dossier in IUCLID. The webinar will cover topics ranging from the installation of the IUCLID 6 application to the creation of a IUCLID 6 registration dossier, including the verification that all required information has been filled-in, using the embedded validation assistant. You will also learn how, under certain conditions, a registration dossier for a member of a joint submission can be created online.
- Date
- 4 October 2016
11:00 - 12:00 EET (GMT +2) - Agenda
- Download agenda [PDF]
- More details
- Webinar page
22 September 2016
11:00 - 12:00 EET (GMT+2)
- Description
-
The webinar focuses on the standard information requirements for REACH registration, including the following endpoints:
- Skin corrosion and irritation
- Serious eye damage and eye irritation
- Skin sensitisation
- Acute toxicity
The webinar explains recent developments in alternative methods and approaches to address these endpoints, including their recent REACH Annex revisions.
The first part of the webinar will focus on information requirements and test methods. The second part gives practical examples on what to do in different situations, depending on the available data.
The webinar is aimed at registrants preparing for REACH registration. Some of the webinar content requires basic knowledge on toxicology and risk assessment and may be complex for a layman audience.
- Date
- 22 September 2016
11:00 - 12:00 EET (GMT+2) - Agenda
- Download agenda [PDF]
- More details
- Webinar page
7 September 2016
11:00 - 12:15 EEST
- Description
-
This webinar is intended for more advanced users of IUCLID 6. It builds on feedback received from users after the IUCLID 6 release and addresses the most frequently asked questions and issues. We will also inform you about upcoming IUCLID service releases. We will conclude the webinar with a live Q&A session where our panellists reply to your questions.
- Date
- 7 September 2016
11:00 - 12:15 EEST - Agenda
- Download agenda [PDF]
- More details
- Webinar page
6 September 2016
11:00 - 12:00 EET (GMT +2)
- Description
-
This webinar gives an overview of some of the key changes implemented in R4BP 3 in October 2016.
It highlights the new possibilities introduced with the extended same biocidal products application process and the new family SPC concept. A description of the new same biocidal product process and a step-by-step demo will provide further insight on the IT implementation.
The webinar is of interest to those companies who would like to take advantage of the new possibilities for the submission of same biocidal products applications and those interested in submitting a biocidal product family application – instead of applying for individual product authorisations.
The content of this webinar is highly technical and previous knowledge of the Biocidal Product Regulation and its tools is recommended.
- Date
- 6 September 2016
11:00 - 12:00 EET (GMT +2) - Agenda
- Download agenda [PDF]
- More details
- Webinar page
20 July 2016
11:00 - 12:10
- Description
-
This is the fourth webinar in a series focusing on practical information to successfully register by the deadline of 31 May 2018.
If you are registering a substance for the first time and you do not know what information you need to submit, you will find this webinar particularly useful.
The webinar will give you an understanding of the type of data you need to collect for the tonnage you want to register. It will also highlight what you should do before generating new data for your substance. Finally, it will give an overview of how to fill in the data gaps, and how the other co-registrants are involved in this common activity.
The webinar will also include a Q&A session where we will respond to your questions.
- Date
- 20 July 2016
11:00 - 12:10 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
21 June 2016
10:00 - 13:00
- Description
-
The webinar introduces you to the new version of the Chemical Safety Assessment and Reporting tool, Chesar 3.0. It is mainly targeted to those who are not yet familiar with the tool but it is also useful for those who want to learn more about the changes between Chesar 2.0 and Chesar 3.0.
To be able to follow this webinar you are expected to know the basics of chemical safety assessment.
The webinar will last 3 hours (from 10 a.m to 13 p.m), followed by a 1 hour break. After the break, we will continue with a question and answer session for up to 2 hours (14 p.m. to 16 p.m.).
Chesar website: https://chesar.echa.europa.eu/
- Date
- 21 June 2016
10:00 - 13:00 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
15 June 2016
11:00 - 12:30
- Description
-
Use maps provide a harmonised way of describing how downstream users use chemicals. Registrants can use this information as input to their chemical safety assessment. They can then provide relevant and realistic conditions for safe use to downstream users in the exposure scenarios that are annexed to the Safety Data Sheet.
This webinar is of interest for downstream user sector organisations and others who are interested in generating sector use maps. It is also relevant for registrants, who want to incorporate the information in dossiers and for downstream users who want to check that their use is covered. Participants will be guided through the use map formats and learn how the concept works in practice.
Questions and answers
- Download [PDF]
- Date
- 15 June 2016
11:00 - 12:30 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
1 June 2016
11:00 - 13:00
- Description
-
This webinar is intended for advanced users of IUCLID.
It will cover server administration for multiple users, new user management features including ‘Instance Based Security' (IBS), merging several IUCLID 5 installations into one IUCLID 6 database and tips for migrating your data. Presentations will be followed by a question and answer session.
- Date
- 1 June 2016
11:00 - 13:00 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
2 March 2016
11:00 - 12:00 Helsinki time
- Description
- This is the third webinar of a series focusing on practical information to successfully register by the deadline of 31 May 2018.If you register a substance for the first time and you do not have previous experience in substance information exchange forum (SIEF) activities and data sharing, you will find this webinar particularly useful. It will give you an understanding of the tasks that the SIEF needs to undertake to prepare a registration dossier.If your substance has already been registered but you will join the existing registration only by 2018, you will find useful information about fair, transparent and non-discriminatory data and cost sharing.Finally, the webinar will include a Q&A session where we will address outstanding issues related to the topic.
- Date
- 2 March 2016
11:00 - 12:00 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
17 February 2016
14:00 - 16:00 Helsinki time
- Description
-
ECHA and Member State Competent Authorities are now in the third year of common screening. In late January every year approximately 200-300 substances are earmarked for manual screening by Member State experts based on an extensive set of algorithms to identify substances that may pose risk to human health or the environment. The short listed substances are grouped in terms of both the suspected hazardous properties and also the REACH/CLP regulatory process that may be the optimal next step. ECHA has recently written to nearly 1 500 companies informing them that their registration dossiers may soon be manually examined by Member State experts to confirm the need for further regulatory action. This webinar will explain the screening process, its timelines, and the criteria for short listing. The webinar will also explain how registrants can influence the manual screening process by updating their dossiers and how they could obtain more information on common screening.
The questions and answers from the webinar are available here.
- Date
- 17 February 2016
14:00 - 16:00 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
10 February 2016
11:00 - 12:30 Helsinki time
- Description
-
This webinar focuses on identifying and sharing best practice on how to provide information on alternatives. The webinar will also inform how the consultations in applications for authorisation work in general. The webinar is based on lessons learned from over 50 consultations carried out so far. It also gives an opportunity for ECHA to get feedback to further develop the consultation process.
The webinar will consist of a presentation from ECHA followed by a panel discussion with Frida Hök from the International Chemical Secretariat (Chemsec), Hugo Waeterschoot from the European Association of the Metals Industry (Eurometaux), Jan Ahlskog from Finsbury International Policy & Regulatory Advisers (FIPRA) and Julius Waller from EPPA.
- Date
- 10 February 2016
11:00 - 12:30 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
2015
18 November 2015
11:00 - 12:00
- Description
-
This is the second webinar of a series focusing on practical information to successfully register by the deadline of 31 May 2018.
If your company does not have previous experience of registering chemicals under the REACH Regulation, you will find this webinar particularly useful. It gives you an understanding of how to retrieve your pre-registrations in REACH-IT and to check if your substance has been already registered. You can then find useful information on how to find the lead registrant or your co-registrants with whom you will need to work together to register jointly. You can also get tips on how to start the work and prepare for being in a substance information exchange forum (SIEF).
Finally, the webinar includes a Q&A session where we addressed outstanding issues related to the topic.
- Date
- 18 November 2015
11:00 - 12:00 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
21 October 2015
11:00 - 12:00
- Description
-
The webinar aims to update downstream users on recent activities that will help them use chemicals safely and fulfil their duties under REACH. The topics will include how downstream users can benefit from the latest work done to improve the information in the supply chain, how to prepare a downstream user chemical safety report and how to notify ECHA on authorised uses. The event will highlight the support that is available to support downstream users.
- Date
- 21 October 2015
11:00 - 12:00 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
22 September 2015
11:00 - 12:30
- Description
-
Replacing hazardous chemicals with safer alternatives can bring substantial benefits to the company, the environment and the health of workers and consumers – all good reasons to substitute them. An additional driver comes from the chemicals legislation. Companies using substances that have been identified as SVHCs under REACH, have to decide whether to apply for a permission to continue using these toxic substances for a limited period of time or to substitute them with safer alternatives.
ECHA and a group of accredited stakeholder organisations have organised a series of webinars aiming to inspire companies to substitute hazardous chemicals and explain how it can be done. All webinars include examples of real life substitution projects. This was the first webinar in the series.
- Date
- 22 September 2015
11:00 - 12:30 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
24 June 2015
11:00 - 12:00 Helsinki time
- Description
-
This is the first webinar of a series focusing on practical information to successfully register by the deadline of 31 May 2018.
The webinar aims to give information to companies that do not have previous experience of registering chemicals under the REACH Regulation. It will give you a basic understanding of which substances in your portfolio need to be registered before the 2018 deadline, the required information and the main costs that need to be budgeted for that purpose. You will also get a clear indication on how to move forward and where to find further information.
Finally, the webinar will include a Q&A session where we will address any outstanding issues related to the topic.
- Date
- 24 June 2015
11:00 - 12:00 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
17 June 2015
11:00 - 14:00 Helsinki time
- Description
-
The webinar provides an introduction to the OECD QSAR Toolbox and its functionalities. Two examples cover endpoints which will be relevant for the third REACH registration deadline in 2018 (e.g. skin sensitisation, aquatic toxicity). The Toolbox is the most comprehensive, widely recognised and freely available platform for data gap filling in regulatory hazard assessment, while avoiding tests. It is used for grouping chemicals into categories, identifying and filling (eco-)toxicological data gaps for the hazard assessment of chemicals. The Toolbox is also very useful for screening and prioritising inventories.
- Date
- 17 June 2015
11:00 - 14:00 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
2014
8 December 2014
11:00 - 12:00 Helsinki time
- Description
-
The webinar covers the classification of mixtures and how information on their safe use can be communicated in the supply chain. It aims to help formulators and importers understand and implement their obligations according to the REACH and CLP regulations relating to mixtures.
- Date
- 8 December 2014
11:00 - 12:00 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
26 August 2014
11:00 - 13:00 Helsinki time
- Description
-
The webinar provides an overview of the ePIC tool used by industry to meet their obligations under the Prior Informed Consent Regulation. It will cover basic aspects of the tool such as the interface, buttons, search functions and other features.
- Date
- 26 August 2014
11:00 - 13:00 Helsinki time - Agenda
- Download agenda [PDF]
- More details
- Webinar page
16 June 2014
- Description
-
Article 95 of the Biocidal Products Regulation is one of the last articles of the regulation but it is the starting point for companies to keep their biocidal products on the market. This webinar is intended to give an overview of the status of the preliminary list published by ECHA, on the data requirements and evaluation principles for the submitted dossiers and on the regulatory aspects.
Note: some of the presentations for this webinar have changed. Please refer to the PDF documents for the latest information.
- Date
- 16 June 2014
- Agenda
- More details
- Webinar page
30 April 2014
- Description
- The webinar gives feedback to registrants about how to address substance identity issues that have been identified as an outcome of ECHA's IT screening campaign. The campaign was undertaken to detect dossiers with substance identity issues, a source of concern as confirmed by the latest evaluation report. The first campaign is focusing on straightforward issues and more complex cases may be covered later.
- Date
- 30 April 2014
- Agenda
- More details
- Webinar page
31 March 2014
- Description
-
This webinar provides feedback to Registrants on how to submit information on chemical substances in the technical dossier to ECHA in compliance with REACH.
Note: this webinar contains out of date information. For the most up-to-date advice, refer to the latest webinars and guidance.
- Date
- 31 March 2014
- Agenda
- More details
- Webinar page
21 March 2014
- Description
- The webinar describes the technical equivalence and chemical similarity processes under the Biocidal Products Regulation and explains their differences. It also gives advice to applicants on how to get the technical equivalence/chemical similarity of their active substance assessed.
- Date
- 21 March 2014
- Agenda
- More details
- Webinar page
5 March 2014
- Description
-
A major update of the Guidance for Downstream Users was published in December 2013. This webinar outlines the structure, the main content of each section and the significant changes in the Guidance. It aims to help the reader to quickly find information in the Guidance that is relevant for his needs.
Further Information
- Date
- 5 March 2014
- Agenda
- More details
- Webinar page
12 February 2014
- Description
- This webinar provides feedback to Registrants on how to submit information on chemical substances in the technical dossier to ECHA in compliance with REACH.
- Date
- 12 February 2014
- Agenda
- More details
- Webinar page
2013
11 September 2013
11:00 - 14:00
- Description
- This webinar provides feedback to Registrants on how to submit information on chemical substances in the technical dossier to ECHA in compliance with REACH.
- Date
- 11 September 2013
11:00 - 14:00 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
14 June 2013
15:00 - 16:30
- Description
-
The webinar provides an overview of the basic concepts of IUCLID as well as an introduction to the new features of IUCLID 5.5
- Date
- 14 June 2013
15:00 - 16:30 - Agenda
- Download agenda [PDF]
- More details
- Webinar page
14 May 2013
11:00 - 14:00
- Description
-
This webinar provides feedback to Registrants on how to submit information on chemical substances in the technical dossier to ECHA in compliance with REACH.
- Date
- 14 May 2013
11:00 - 14:00 - Agenda
- More details
- Webinar page
2 May 2013
11:00 - 14:00
- Description
-
The webinar will provide information to registrants on the type of information to be included in a REACH registration dossier for a substance with nanoform(s).
Note: this webinar contains out of date information. For the most up-to-date advice, refer to the latest webinars and guidance. - Date
- 2 May 2013
11:00 - 14:00 - Agenda
- More details
- Webinar page
8 April 2013
11:00 - 14:00
- Description
-
The webinar gives an overview of when downstream users need to report to ECHA, including when to report classification differences. The two options for reporting are outlined, namely using the web-form or submitting a IUCLID dossier via REACH-IT. How to use the webform and the conditions of use template is described in more detail. How ECHA, in turn, uses this information is outlined.
- Date
- 8 April 2013
11:00 - 14:00 - Agenda
- More details
- Webinar page
20 March 2013
11:00 - 14:00
- Description
-
The aim of the webinar is to explain the restriction procedure relating to five cobalt salts (cobalt sulphate, cobalt dichloride, cobalt dinitrate, cobalt carbonate and cobalt diacetate) and how the preliminary study on the uses of these cobalt salts conducted by ECHA contributes to it.
- Date
- 20 March 2013
11:00 - 14:00 - Agenda
- More details
- Webinar page
5 March 2013
11:00 - 14:00
- Description
-
Focuses on the key steps needed to successfully submit a member registration dossier by the 31 May 2013.
- Date
- 5 March 2013
11:00 - 14:00 - Agenda
- More details
- Webinar page
25 February 2013
- Description
-
This webinar focuses on the key technical steps needed to successfully submit a lead registration dossier by the 31 May 2013.
- Date
- 25 February 2013
- Agenda
- More details
- Webinar page
28 January 2013
11:00 - 14:00
- Description
-
This webinar provides feedback to Registrants on how to submit information on chemical substances in the technical dossier to ECHA in compliance with REACH.
- Date
- 28 January 2013
11:00 - 14:00 - Agenda
- More details
- Webinar page
2012
23 November 2012
- Description
-
The webinar presents an overview of a new feature in REACH-IT which supports potential and existing registrants in sharing data and preparing joint submissions. The new feature provides real time information on identity, contact details and roles of co-registrants who have received a registration number or an inquiry number, making it easier for them to share common responsibility and interests regarding REACH.
- Features of the Co-Registrants Page (live demo) - Daniel Sompolski - [Play recording]
- Date
- 23 November 2012
- Agenda
- More details
- Webinar page
22 November 2012
- Description
- Focus on generalities, use of TCC tool, process description, how to avoid unexpected fees, fee calculator tool, invoice information in REACH-IT
- Date
- 22 November 2012
- Agenda
- More details
- Webinar page
9 November 2012
- Description
- Business rules: what they are and how to pass them; how to fill a dossier header, dossier submission
- Date
- 9 November 2012
- Agenda
- More details
- Webinar page
30 October 2012
- Description
-
This webinar will provide information to Registrants on the type of information to be included in a REACH registration dossier for a substance with nanoform(s).
Note: this webinar contains out of date information. For the most up-to-date advice, refer to the latest webinars and guidance. - Date
- 30 October 2012
- Agenda
- More details
- Webinar page
19 October 2012
- Description
-
Focus on substance datasets, dossier creation in IUCLID, creation of Joint Submission in REACH-IT (lead registrant), confirming membership in Joint Submission in REACH-IT (member registrants), submission of registration dossier in REACH-IT
- Date
- 19 October 2012
- Agenda
- More details
- Webinar page
5 October 2012
- Description
-
This webinar gives an overview of the purpose of substance evaluation under REACH and its practical implementation. It provides important tips for the Registrants how to cooperate with ECHA and the evaluating Member States if their substance is selected for substance evaluation.
- Date
- 5 October 2012
- Agenda
- More details
- Webinar page
27 September 2012
- Description
-
This webinar provides feedback to Registrants on how to submit information on chemical substances in the technical dossier to ECHA in compliance with REACH.
- Date
- 27 September 2012
- Agenda
- More details
- Webinar page
6 September 2012
- Description
-
Key concepts for registrants on the rules of confidentiality claims and the dissemination of information post-registration.
- Date
- 6 September 2012
- Agenda
- More details
- Webinar page
11 June 2012
- Description
-
Webinar targeted towards small and medium sized companies providing an overview of the SME definition and its benefits with respect to the REACH regulation. The webinar aims to cover the SME verification process and available tools and support for SMEs in preparing their registration dossiers.
- Date
- 11 June 2012
- Agenda
- More details
- Webinar page
21 May 2012
- Description
-
The webinar gives you an overview of the functionalities of ECHA's Chemical Safety Assessment and Reporting Tool (Chesar), an in depth live demonstration of the beta-version as well as information for potential users interested in trying out the application before its release in June.
Presentations
Introduction - Roberta Bernasconi - [Play recording]
In-depth live demonstrations of Chesar 2.0 Beta (PartI I) - Helene Magaud - [Play recording]
In-depth live demonstrations of Chesar 2.0 Beta (Part II) - Helene Magaud - [Play recording]
Information for potential users interested in trying out the application before its release - Roberta Bernasconi - [Play recording]
- Date
- 21 May 2012
- Agenda
- More details
- Webinar page
26 April 2012
- Description
-
This webinar gives an overview of the purpose of the chemical safety assessment under REACH and the information expected in a chemical safety report. It covers:
- Lessons learned from the first wave of chemical safety reports received at ECHA
- Tips on selected issues
- How can Chesar support registrants in documenting the chemical safety assessment in an efficient and transparent manner?
- Date
- 26 April 2012
- Agenda
- More details
- Webinar page
27 March 2012
- Description
-
The webinar is aimed to member registrants and it offers information on the following topics:
- Introductory part on the SIEF process
- Key messages on the importance of proper substance identification
- Data sharing and related disputes.
Presentations
Introduction to the webinar – Laurence Hoffstadt - [Play recording]
Introduction to substance identification - Paweł Figiel - [Play recording]
Substance identification – Examples - Benedek Poor - [Play recording]
Activities in SIEF & Obligations of registrants - Nikolaos Georgiadis - [Play recording]
Data sharing negotiations – ECHA's experience - Diana Antal - [Play recording]
Submission of a data sharing dispute - Daniel Sompolski - [Play recording]
Key messages and conclusions - Laurence Hoffstadt - [Play recording]
- Date
- 27 March 2012
- Agenda
- More details
- Webinar page
29 February 2012
- Description
-
The webinar focuses on dealing with data gaps and alternative methods
Presentations
Introduction - Marco Valentini
Information requirements under REACH - David Bell
Evaluation & Reporting of Data: Robust Study Summaries and Study Summaries - Marco Valentini -
Read-Across, Grouping and Categories: possibilities and limitations - Karel de Raat -
Key messages - Marco Valentini
- Date
- 29 February 2012
- Agenda
- More details
- Webinar page
29 February 2012
- Description
-
The webinar focuses on compiling the substance dataset
Presentations
Intro – David Bell
Weight of Evidence - David Bell
How to use in vitro data to fulfil REACH information requirements - Laura Rossi
Regulatory Use of (Q)SARs under REACH - Tatiana Netzeva
Key messages Information Requirements II - David Bell
- Date
- 29 February 2012
- Agenda
- More details
- Webinar page
17 January 2012
- Description
-
The webinar aims to give you information on the following topics:
- Data sharing obligations: legal framework and SIEF activities
- Disagreements on who shall perform the missing test
- Disputes for (late) pre-registered substances
- Disputes for inquired substances
- Best practice and tips for successful data sharing
- Submission of the data sharing disputes
Presentations
Data Sharing & Data sharing disputes, Introduction - Laurence Hoffstadt - [Play recording]
Data Sharing Obligations - Nikolaos Georgiadis - [Play recording]
Data Sharing Disputes - Daniel Sompolski - [Play recording]
Best Practice - Diana Antal - [Play recording]
Key messages and Conclusion - Laurence Hoffstadt - [Play recording]
; - Date
- 17 January 2012
- Agenda
- More details
- Webinar page
2011
16 November 2011
- Description
-
The webinar provides practical information for understanding how the technical completeness check (TCC) plug-in works. The webinar was presented to the network of National Helpdesks (HelpNet).
Webinar topics:
- Differences between business rules, technical completeness and substance identification checks
- Difference between failures and warning messages.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.Examples and tips
- Date
- 16 November 2011
- Agenda
- More details
- Webinar page
27 September 2011
- Description
-
Practical information to get started with IUCLID, including:
- How to download and install IUCLID
- Getting familiar with the tool and its environment
Video tutorials
These videos explain how to download and install the required software for a standalone environment of IUCLID 5.
- Java – Robin Allen
- PostgreSQL – Robin Allen
- The installer for standalone IUCLID 5 in MS Windows. This provides all the plug-ins - Robin Allen
- Manual installation of an optional plug-in (TCC) – Sophia van der Made
- Date
- 27 September 2011
- Agenda
- More details
- Webinar page
31 May 2011
- Description
- Practical information on how to complete a downstream user report using IUCLID 5 and successfully submit it to ECHA via REACH-IT.
- Date
- 31 May 2011
- Agenda
- More details
- Webinar page
25 May 2011
- Description
-
Basis of the inquiry process covering:
- Assessment of the substance identity
- Aspects of data sharing
- Common deficiencies ECHA has identified in the inquiry dossiers related to substance identification and verification of substance identity
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 25 May 2011
- Agenda
- More details
- Webinar page
19 May 2011
- Description
-
This webinar provides legal background and practical information on how to prepare and submit a notification of a Substance of Very High Concern in articles using IUCLID and REACH IT.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 19 May 2011
- Agenda
- More details
- Webinar page
2010
14 December 2010
- Description
-
Webinar date
14 December 2010
Summary
This webinar provides tips on how to use the different IT tools available for notifiers to submit successfully their classification and labelling notifications by the deadline on 3 January 2011.
Presentations
Introduction - Doris Thiemann
XML Bulk Tool - Tuomo Honkanen
IUCLID 5 - Sophia van der Made
Online Submission - Rubén González Vida
Read your submission report and retrieve what you have submitted - Rubén González Vida
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 14 December 2010
- Agenda
- More details
- Webinar page
9 November 2010
- Description
-
Best practice when entering the invoice-related information in the registration dossier to ensure a prompt processing of the payment and, therefore, a fast issue of the registration number.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 9 November 2010
- Agenda
- More details
- Webinar page
5 November 2010
- Description
-
This webinar offers further assistance to any companies who may still be unfamiliar with the registration process and it focuses on the key technical steps to ensure the successful submission of a member registration dossier by the 30 November 2010 deadline.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 5 November 2010
- Agenda
- More details
- Webinar page
8 September 2010
- Description
-
How to be more effective when working with REACH IT, in particular how to pass the 'business rules'. Tips on how to successfully register by using examples of common mistakes and how these can be avoided.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 8 September 2010
- Agenda
- More details
- Webinar page
28 June 2010
- Description
-
The following webinar gives tips on how to pass the business rules verification and explains the most common mistakes.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 28 June 2010
- Agenda
- More details
- Webinar page
21 June 2010
- Description
-
This webinar provides a status update of the REACH-IT and IUCLID 5 tools, and also gives information on preparing a classification and labellingnotification using these tools.
Some of the information and screenshots included in the webinar presentations may be inaccurate after the latest updates of REACH-IT, IUCLID or other software tools. Please refer to the most recent webinars for the most up-to-date information.
- Date
- 21 June 2010
- Agenda
- More details
- Webinar page