EMA consults on risk

March 2, 2016

THE European Medicines Agency has published a revised module on “the Good Pharmacovigilance Practices (GVP) on risk management systems,” with a public consultation now open for submissions until 31 May. It’s the first major revision of the GVP since its 2012 launch, and is based on experience gained since the EMA’s Pharmacovigilance Risk Committee started its operations. Changes include clarification of the activities a risk management plan should focus on during the life cycle of a product, ensuring that “planning of activities directs resources to areas where the need for additional information and risk minimisation is greatest”. See ema.europa.eu for details.

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Pharmacy Daily | EMA consults on risk

EMA consults on risk

Other recent headlines

WA group stocks vapes

Fujitsu to protect against cyber threats

PD breaking news – Queensland pharmacies scope of practice pilot expanded

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES