Pharmacovigilance Risk Assessment Committee (PRAC)

The Pharmacovigilance Risk Assessment Committee (PRAC) is the European Medicines Agency's (EMA) committee responsible for assessing and monitoring the safety of human medicines. The Committee meets once a month. EMA publishes the agendas, minutes and highlights of its plenary meetings.

For full details, see the PRAC rules of procedure and work plan.

Publication of PRAC agendas, minutes and highlights

EMA's Pharmacovigilance Risk Assessment Committee (PRAC) meets once a month. EMA publishes the agendas, minutes and highlights of its plenary meetings.

PRAC publication times

Meeting highlights

Friday after Committee plenary

Agendas

Before start of Committee plenary

Minutes

After Committee plenary where minutes are adopted

Useful information

Upcoming PRAC meetings

SEE ALL EVENTS

PRAC meeting highlights

SEE ALL NEWS

PRAC agendas


PRAC minutes


Share this page