The revised ATMP guideline on safety and efficacy follow-up and risk management has been released for a 3-month public consultation (deadline of 30th April).
EMA would be pleased to receive any HTA comments in respect of the post-authorisation safety and efficacy studies’ endpoints.
Please see the links below.
Guideline on safety and efficacy follow up RMP for ATMP: https://docs.eudra.org/webtop/drl/objectId/090142b283cccb2e