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ECHA Urges Companies to Get Ready for New REACH Requirements for Nanomaterials

The European Chemicals Agency (ECHA) issued a press release on October 8, 2019, reminding companies that by January 1, 2020, companies must provide more information on nanomaterials on the European Union (EU) market under the Registration, Evaluation, Authorization and Restriction of Chemicals (REACH) regulation.  The new information requirements concern companies that manufacture or import nanoforms of substances that are subject to registration under REACH.  As reported in our December 4, 2018, blog item, the European Commission (EC) amended several REACH Annexes to introduce clarifications and new provisions for:

  • Characterization of nanoforms or sets of nanoforms covered by the registration (Annex VI);

  • The chemical safety assessment (Annex I);

  • Registration information requirements (Annexes III and VII-XI); and

  • Downstream user obligations (Annex XII).

ECHA states that the purpose is to ensure that companies provide enough information to demonstrate the safe use of their nanoforms for human health and the environment.  The amendments apply to all the new and existing registrations covering nanoforms.  ECHA states that it expects registrants to update their existing dossiers with nanoform-specific information by January 1, 2020.

ECHA notes that its new nano-specific guidance is intended to help companies comply with the changes in Annex VI.  In addition, ECHA is updating the guidance on read-across between nanoforms or sets of nanoforms to reflect the changes.  ECHA intends to have both documents ready by the end of 2019.  ECHA is also updating the 2017 ECHA guidance for human health and the environment.  According to ECHA, the Organization for Economic Cooperation and Development (OECD) is revising some of its existing test guidelines used under REACH to ensure that data generated on nanoforms is reliable and meets regulatory standards.  An overview of the revised REACH Annexes and the available test methods is available on the EU Observatory for Nanomaterials (EUON) website.

On October 30, 2019, the International Uniform Chemical Information Database (IUCLID) will be updated with new data fields for reporting the characteristics of nanoforms and sets of nanoforms.  Beginning October 30, 2019, registrants who intend to submit registrations covering substances in nanoform must provide complete characterization information on their nanoforms or sets of nanoforms.  According to ECHA, the completeness check will include a verification that the sets of nanoforms are accompanied by a justification for creating the set.  As before, the IUCLID tool will include the means to link these nanoforms or sets of nanoforms with the relevant data on their properties and hazards in the other parts of the dossier.  ECHA states that companies submitting information on nanoforms must use the new version of IUCLID because it is not possible to prepare a successful submission with previous versions.

As reported in our September 27, 2019, blog item, ECHA is hosting a webinar on November 12, 2019, to introduce the guidance on identifying and reporting nanoforms and sets of nanoforms.  During the webinar, companies will have the opportunity to get advice directly from ECHA’s experts.  ECHA notes that its help desk is available to assist companies prepare for the new requirements.

©2020 Bergeson & Campbell, P.C.National Law Review, Volume IX, Number 282


About this Author

Lynn Bergeson, Campbell PC, Toxic Substances Control Act Attorney, federal insecticide lawyer, industrial biotechnology legal counsel, Food Drug Administration law
Managing Partner

Lynn L. Bergeson has earned an international reputation for her deep and expansive understanding of the Toxic Substances Control Act (TSCA), the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), European Union Registration, Evaluation, Authorization and Restriction of Chemicals (REACH), and especially how these regulatory programs pertain to nanotechnology, industrial biotechnology, synthetic biology, and other emerging transformative technologies. Her knowledge of and involvement in the policy process allows her to develop client-focused strategies whether...

Carla Hutton, Bergeson Campbell PC, global regulatory attorney, public health activists lawyer, metals industry legal counsel, Toxic Substances Control Act law
Regulatory Analyst

Since 1996, Carla Hutton has monitored, researched, and written about regulatory and legislative issues that may potentially affect Bergeson & Campbell, P.C. (B&C®) clients. She is responsible for creating a number of monthly and quarterly regulatory updates for B&C's clients, as well as other documents, such as chemical-specific global assessments of regulatory developments and trends. She authors memoranda for B&C clients on regulatory and legislative developments, providing information that is focused, timely and applicable to client initiatives. These tasks have proven invaluable to many clients, keeping them aware and abreast of developing issues so that they can respond in kind and prepare for the future of their business.

Ms. Hutton brings a wealth of experience and judgment to her work in federal, state, and international chemical regulatory and legislative issues, including green chemistry, nanotechnology, the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), the Toxic Substances Control Act (TSCA), Proposition 65, and the Registration, Evaluation, Authorization and Restriction of Chemicals (REACH) program.