PRAC meeting highlights 11-14 April 2023
11/04/2023
Medicines for human use
Pharmacovigilance risk assessment committee (PRAC)
The European Medicines Agency's Pharmacovigilance Risk Assessment Committee (PRAC) is responsible for assessing and monitoring safety issues for human medicines.
The PRAC did not start or conclude any referral procedures during the April 2023 meeting. More information on all safety reviews currently under evaluation is provided in the 'Ongoing referrals' table.