Pharmacovigilance Risk Assessment Committee (PRAC) Meeting Highlights

Notice type: 3rd Party Publications

Date: 12/04/2024

 


Background Information Or Related Documents:

The Pharmacovigilance Risk Assessment Committee (PRAC) is responsible for assessing and monitoring safety issues for human medicines. Its recommendations are considered by the Committee for Medicinal Products for Human Use (CHMP) when it adopts opinions for centrally authorised medicines and referral procedures and by the Co-ordination Group for Mutual Recognition and Decentralised Procedures – Human (CMDh) when it provides a recommendation on the use of a medicine in Member States.

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Meeting highlights from previous years




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