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Pharmacovigilance

UK MHRA sets out goals for pharmacovigilance

Delegates at a UK Medicines and Healthcare products Agency (MHRA) seminar on pharmacovigilance on 6 February 2007 were updated on the agency's work relating to issues surrounding medicines safety, including the introduction of Volume 9A of the rules governing medicinal products in the European Union (EU). Speakers included representatives from the MHRA itself and from industry.

The first session began with June Raine, director of vigilance and risk management of medicines at the MHRA, discussing the...

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