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More informationMeeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 21-24 February 2022
EMA’s PRIority Medicines (PRIME) scheme has had a positive impact on the authorisation of new medicines.
New bill seeks to revamp FDA’s accelerated approvals programme
Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 15-16 February 2022
MHRA Good Practice Symposia Week (7 to 11 March 2022)
Blog Post - Regulators’ experience of clinical trials during the Covid-19 pandemic (Part 3) – looking forward
The next MHRA Board Meeting held in public will be conducted virtually by webinar on Tuesday, 15 March 2022 from 10.00 until 12.30 hrs. (GMT).
There are currently 5 separate events planned for March 2022.
EMA has published an overview of its key recommendations in 2021 on the authorisation and safety monitoring of medicines for human use.
In 2022, EMA will offer short talks for clinical trial sponsors focused on CTIS functionalities.