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EMA and EATRIS present: Navigating the Regulatory Requirements for ATMPs
Developers of ATMPs face challenges due to the complexity of these products and may encounter challenges in navigating – and complying with – regulatory  requirements. The development programme can differ substantially from that of chemical and simpler biologicals, and existing guidelines may not apply or have additional requirements.

In this webinar we will discuss a non-linear development programme and share developmental scientific and regulatory issues commonly encountered in ATMP dossiers.

The Webinar is hosted by the ADVANCE Programme and EATRIS - David Morrow in collaboration with the European Medicines Agency - Charlotte Bakker.

Nov 29, 2021 01:00 PM in Amsterdam

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