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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.

Q&A transcript

ECHA poison centres website

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.

More about the new IUCLID >>

Recording

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.

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.

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.

More about REACH 2018

Watch our REACH 2018 webinars

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.

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Webinar Q&A transcript

Agenda

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.

More about REACH 2018 

Watch our REACH 2018 webinars 

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

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.

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

Call for evidence

ECHA to consider restrictions on the use of oxo-plastics and microplastics, ECHA news 17 January 2018

Q&A from the online information session

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

Watch all REACH 2018 webinars

Note: Some parts of this webinar are no longer up to date. For the latest information, refer to our more recent webinars on IUCLID.

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.

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

Q&A on screening of substances of potential concern >>