The webinar introduces the latest version of IUCLID 6 (v7.10.1) released on 30 October 2023.

This version is fully compatible with the May release of IUCLID and brings a series of new functionalities as well as fixes and improvements.

During the webinar, we will address topics such as:

• Performance improvements
• Latest improvements for the transition towards using IUCLID for ‘Summary of Product Characteristics’ under the EU Biocidal Products Regulation
• Improvements to data entry
• IUCLID filtering and report generator enhancements
• Helpdesk advice

Full details of the release can be found here.

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Join us for an informative webinar that will equip notifiers of industrial use only mixtures with essential knowledge ahead of the compliance date on 1 January 2024.

This webinar gives an overview of the changes to the CLP Regulation and their potential impact on poison centre notifiers. Gain valuable insights into the submission format, tools, and support that will facilitate your compliance process.

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Subscribe to our channel to get notified before the broadcast starts.

Programme

Useful links

• Compliance date for industrial use only mixtures approaching - January 2024 - ECHA news, 12 June 2023
• Guidance on harmonised information relating to health emergency response - Annex VIII to CLP [PDF] [EN]

Welcome to the second part of our webinar series on the new ECHA public data availability system. This webinar continues from our first webinar organised in April 2023.

In this session, we will guide you through the progress made in the development of the new system, that will replace our existing chemicals database. Through a live demonstration, we will showcase the features of its initial release and provide updates on the transition timeline.

ECHA maintains the largest chemicals database in the European Union, integrating industry-submitted data with regulatory information. In 2022, our database received over 30 million pageviews and we are on track for 50 million pageviews in 2023.

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Given the growing volume and diversity of data to be made available, ECHA is introducing a new system. The system will be phased in over the coming years, starting with REACH registration data and progressing to the Classification and Labelling Inventory, followed by regulatory data. The aim of this webinar series is to inform you about the upcoming changes and help you prepare for them.

Join us for this informative session, as we outline the future of our chemicals database.

We have now published more than 110 reports on assessments of regulatory needs in nearly two years, covering about 3 000 substances. This webinar further explains our approach to these assessments, upcoming improvements for how we inform registrants about published assessments of regulatory needs for their substances, and how you can react in case your substance is addressed in a group assessment.

Join the event to also learn about the role of the assessments of regulatory needs in the context of ECHA’s Integrated Regulatory Strategy and the formal processes under REACH and CLP.

We will address your questions on the group assessment work, how you can prepare and what to do if we propose regulatory actions for one of your substances.

Watch the webinar

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Programme

Useful links

• Addressing chemicals of concern - ECHA

The webinar introduces the latest version of IUCLID (version 6.7) to be released at the end of May 2023.

This version reflects the first format changes since October 2021, and contains the latest Data Reporting standards as agreed at the OECD level, as well as updates to other formats that support Data Reporting for specific regulations in EU, New Zealand and Australia.

This version also contains a range of improvements to IUCLID functionalities that will support the data entry and export, as well as the re-use of data (see the highlights here).

The webinar gives an overview of the format changes and new functionalities.

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Programme

We are revamping our regulatory submission systems: REACH-IT, ePIC, R4BP 3 and the ECHA Submission Portal.

These systems allow companies to comply with their obligations under REACH, CLP, PIC, the Biocidal Products Regulation, and the Waste Framework Directive.

We are building a unified portal for industry, centralising interactions between duty holders across various regulatory frameworks.

In this event we present the overall approach and next steps.

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Watch the webinar

Programme

Substitution and analysis of alternatives of the most hazardous biocidal active substances are topics of growing interest. This webinar features several tools and initiatives that support companies in moving to safer alternatives. The event is of particular interest for applicants of biocidal active substances, downstream users, suppliers of alternatives, authorities and consultants.

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Watch the webinar

Programme

More on the topic:
Substitution to safer chemicals
New framework guidance and reporting template published in January 2023
Implementation note 

Are you using ECHA’s chemicals database? If your answer is yes, this webinar is for you. In this first session, we cover our plans for the new data availability system which will gradually replace our current chemicals database. We will have further, more detailed sessions later in the year as the development advances. 

We maintain the largest database on chemicals in the European Union. This database brings together chemicals data submitted by industry and information generated by the regulatory activities of ECHA and authorities. In 2022 the chemicals database received over 30 million views.

Due to an increasing amount and variety of data to be made available, we are building a new data availability system. The new solution will be rolled out in several steps during the next couple of years. We will start with REACH registration data at the end of this year, followed by the classification and labelling inventory and regulatory data.

The aim of this webinar is to let you know what to expect and to help you prepare for the changes.

Questions and answers

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Watch the webinar

Programme

Germany, the Netherlands, Denmark, Norway and Sweden have proposed a REACH restriction to address the risks to the environment and human health from the manufacture, placing on the market and use of per- and polyfluoroalkyl substances (PFAS).

A six-month consultation on the proposal started on 22 March 2023.

This webinar explains the restriction proposal, how the REACH restriction process works and how to participate in the consultation.

Questions and answers

Download Q&A (part I - consultation, opinion-making, process)
3 May 2023

Download Q&A (part II - content of the proposed restriction)
28 June 2023

Recording

Programme

Background

Per- and polyfluoroalkyl substances (PFAS) are very persistent in the environment. If their releases are not minimised, people, plants and animals will be increasingly exposed, resulting in harmful effects.

Germany, the Netherlands, Denmark, Norway and Sweden have drawn up a proposal to restrict PFASs in Europe (currently more than 10 000 substances). The authorities estimate that around 4.5 million tonnes of PFAS will end up in the environment over the next 30 years unless action is taken.

The proposed restriction on PFAS is set to be one of the largest ever on chemical substances in the EU.

More

• ECHA seeks input on proposed PFAS restriction, ECHA news - 22 March 2023
• ECHA publishes PFAS restriction, ECHA news - 7 February 2023
• ECHA receives PFASs restriction proposal from five national authorities, ECHA news - 23 January 2023
• Video: Media briefing – Banning PFASs in the EU, 7 February 2023
• More on PFAS

Disclaimer

Parties are reminded that only the Court of Justice of the European Union can give authoritative interpretations on Union law. The European Chemicals Agency does not accept any
liability with regard to the use that may be made of the information provided in the webinar. Use of the information remains the sole responsibility of the user.

The European Commission has revised some of the information requirements for registering chemicals under REACH (Action 1, Action 2). This webinar focuses on the new and amended completeness check rules brought by this revision to help you prepare a complete registration dossier. We also give you an overview of the process in general.

Completeness check will be aligned with the revised information requirements in May 2023, after the next major IUCLID release.

Update 12 April 2023: Following a postponement of the next IUCLID release, the new and amended completeness checks will take effect as of 1 June 2023.

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List of new and amended completeness check rules

Programme

The webinar introduces the latest IUCLID 6 version published on 31 October 2022. This release contains several improvements to the web user interface as part of our long-term plan to move to one interface for everyone using IUCLID. The changes include for example supporting you to better review and filter the data you are importing into your IUCLID instances.

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Programme

The Data Uploader can be used to convert chemical data into IUCLID format. It is especially useful for converting legacy toxicity data into harmonised templates that can be stored in a IUCLID database. It can be used for example by owners of chemical databases to share their data in an internationally recognised format.

It is developed as a KNIME Analytics Platform plug-in, using several workflow nodes:

• Connection to a IUCLID database
• Selection of relevant IUCLID documents and fields
• Mapping with an external data source
• Validation of the data against the IUCLID format
• Generation of IUCLID files (.i6z)
• Uploading to IUCLID
• Incremental update

In this webinar, we will help you get started with the Data Uploader and guide you through the different workflow steps.

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Programme

Questions and answers received during the webinar.

The webinar presents the latest features of REACH-IT (version 3.14) and gives an overview of future developments planned for the following months.

We will also give practical examples on the new requirement where only representatives need to identify the non-EU manufacturers they represent.

You will also find out how to ensure that there are separate accounts for each of the non-EU manufacturers you represent.

Questions and answers received during the webinar.

The webinar introduces the latest IUCLID 6 (version 6.14) released on 26 April.

This version brings changes to the web interface that improve how you can manage, view, and edit data for your substances, mixtures and articles.

The new version also has single sign on support (SSO) and introduces PostgreSQL as an additional database option.

Questions and answers received during the webinar.

This webinar introduces the QSAR Toolbox together with practical advice on how to use its new and essential features. It gives an overview of future developments planned for the QSAR Toolbox in the coming years.

You will learn how it connects to IUCLID and get hands on advice for using it to support read-across studies for REACH information requirements.

The US Environmental Protection Agency also presented its activities on the QSAR toolbox.

ECHA together with the OECD have managed the QSAR toolbox for over a decade. It is free software that supports reproducible and transparent chemical hazard assessment using non-animal methods.

Programme

ECHA has investigated the environmental and health risks posed by using PFASs in firefighting foams at the request of the European Commission. The Agency concluded that an EU-wide restriction is justified as the risks posed by PFASs are currently not adequately controlled and releases should be minimised.

A six-month consultation starts on 23 March and will be open for anyone to give evidence-based comments on the restriction proposal.

This info session explains the restriction process and helps those interested to take part in the consultation.

Questions and answers from the event

Since 5 January 2022, certain hazardous chemicals in mixtures used for tattooing and permanent make-up are restricted in the EU.

The European Commission and ECHA organised an online information session to address technical questions that industry, such as ink formulators and tattoo artists, might have on the implementation of the restriction. The aim was to help those impacted to meet the new legal requirements set by Annex XVII of the EU’s chemicals legislation, REACH.

Questions and answers

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Programme

More

• REACH Restriction on hazardous substances in tattoo inks
• Restriction proposal and process
• More about tattoo inks and permanent make-up

The webinar explains how ECHA assesses the regulatory needs of groups of substances and how this approach helps speed up regulatory action for substances of concern – and what information ECHA has started to publish to better inform companies and citizens about the foreseen action towards a safer use of chemicals.

Questions and answers from the event.

Agenda

Update June 2022

• Practical guide
• Results of the survey

This event was a follow-up of our previous webinar on how to submit harmonised classification and labelling dossiers that took place on 26 May 2021.

It focussed on:

• Results of the survey on the challenges dossier submitters face in preparing harmonised classification and labelling dossiers
• Feedback on the practical guide that was collected after the previous webinar

Other presentations included biocides, read across and EFSA on plant protection products.

Programme

Questions and answers from the webinar

The webinar is of interest to all Member State harmonised classification and labelling dossier submitters for REACH chemicals but also for active substances used in biocides and plant protection products.

If you have any questions, contact us: classification (at) echa.europa.eu.

This webinar will explain how consumers, waste operators and article suppliers can make the best use of the SCIP dissemination portal when searching for data on articles containing substances of very high concern that are on the EU market. 

Questions and answers from the event.

The webinar presents the experience of different stakeholders using the QSAR Toolbox. After a status overview given by OECD, ECHA will present how the QSAR Toolbox results are used and assessed in different REACH processes. The webinar will continue with presentations from academia (Danish Technical University, DTU) and governmental organisations (Italian National Institute of Health, ISS; Environment and Climate Change Canada, ECCC; National Institute of Technology and Evaluation, NITE Japan) about their uses of the QSAR Toolbox.

The OECD QSAR Toolbox is a free software for screening and assessing chemical substances that uses computational methods as an alternative to animal testing. It is used worldwide by over 25,000 users such as regulatory authorities, industry, academia, and non-governmental organisations. The Toolbox is developed by ECHA and OECD. 

Questions and answers from the event.

This webinar details all the latest changes and improvements following the October 2021 release of the poison centre notification (PCN) format and IT solution. We provide more information on the group submission process, as well as cover the coming changes such as the disable submission functionality. 

Questions and answers from the event.

ECHA started to manually verify the completeness of chemical safety reports on 1 March 2021. After the first months of the new checks, we are now able to provide targeted advice on the most common reasons for incompleteness. 

Join our webinar to hear about our observations and receive useful tips on how to avoid failing the completeness check. Use the opportunity to ask questions from our experts. 

Questions and answers from the event

Questions and answers received during the webinar.

This webinar introduces the latest version of IUCLID 6, released on 27th October.

IUCLID has two scheduled updates a year. This update contains a number of enhanced features to support those who need to submit data for regulatory purposes in the IUCLID format. This applies to jurisdictions both inside and outside the EU.

We will present an overview of the important changes in this release of IUCLID. We will provide an update on what has changed with the IUCLID report generator and give an overview of how IUCLID’s default reports can be used. We will also share some guidance on where to find IUCLID’s support material and give a live demo of the main changes.

More about IUCLID

The webinar covers the requirements for the use of QSAR results as adaptations to standard information in REACH registrations. It also shows how ECHA evaluates the compliance of QSAR information. Finally, it illustrates the most common issues found in QSAR studies included in REACH dossiers and how they are addressed in ECHA’s decisions. The webinar is particularly addressed to REACH registrants, who may include QSAR results in their registration dossiers and to stakeholders interested in learning about ECHA’s methods on evaluating QSAR results.

• Questions and answers from the event

This online information session presents the practical guide How to submit CLH dossiers. The 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. 

Questions and answers from the event.

Programme 

Moderator: Stella Jones, Head of Unit, Hazard I

This webinar introduces the latest IUCLID 6 version (5.15.0) released on 28 April 2021.

IUCLID is updated twice a year. This April service release contains the remaining features of the web interface to be implemented: User and Report management, as well as a number of configurations to support users preparing dossiers for EU REACH, CLP, Plant Protection Products (PPP) and the Waste Framework Directive (SCIP).

In this webinar, we will focus on presenting the latest IUCLID web interface features and improvements, and how IUCLID has been configured in particular to support PPP users. In addition, we will have a segment on how the web interface can be best utilised by EU REACH users.

Questions and answers from the event.

• More about IUCLID

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.  

Questions and answers from the event.

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

Presentations

• All slides into one [PDF] - Mark Blainey, Christiaan Logtmeijer, Peter Simpson

• You are new to dossier preparation
• Your dossier is failing validation rules
• You need to make an update to your notification  

Presentations

• All slides in one [PDF] - Heidi Rasikari, Daniele Ape, Claudia Rimondo

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

Presentations

• All slides in one [PDF] - Eduardo López, Tuomas Aitasalo, Reka Vataja

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

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).

Webinar Q&A

Programme

Note: Some of the information included in this webinar may be inaccurate. Refer to more recent support material for the most up-to-date information.

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.

• More about IUCLID 
• Questions and answers [PDF]

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.

More about SCIP

Date: 19 Nov 2020
Time: 11:00 – 15:00 Helsinki Time (EET, GMT+2)

Agenda

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]

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

• Webinar Q&A [PDF]

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

More on PFAS

• Presentations (All slides in one) [PDF]
• Questions and answers [PDF]

Date: 29 October 2020

Time: 13:30–15:30 CET, GMT+1

Agenda

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

Biocidal product families

Questions and answers

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.

Webinar Q&A

Agenda

Understanding PIC

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
   

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.

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.

Webinar Q&A

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.

Webinar Q&A

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.

• Webinar Q&A
• More about EUCLEF

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.

Questions and answers

Agenda

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

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.

Q&A transcript

Agenda

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.

Podcast

Interview with Karine Fiore, Regulatory and Socio-Economic Projects Manager from the French Agency for Food, Environmental and Occupational Health & Safety (ANSES).

Agenda

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.

Webinar questions and answers

Agenda

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

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.

Webinar questions and answers