European Medicines Agency phasing out follow-up measures for MAs

2 August 2012

The European Medicines Agency this week issued a statement reminding marketing-authorization holders for medicinal products that it is phasing out follow-up measures to marketing authorizations.

In the context of an exercise on quality of opinions started together with the European Commission, the Agency and its Committee for Medicinal Products for Human Use (CHMP) have started to classify all post-authorization measures for human medicines as one of the following:

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