European Commission publishes latest pharma GMP regulation

Published: 21-Jan-2015
Regulatory

For active substances for medicinal products for human use


The European Commission has released a text of the latest secondary regulations underpinning European Union (EU) directive 2001/83/EC on good manufacturing practice for active substances for medicinal products for human use.

The latest regulation, approved by the Commission, without reference to the European Parliament and EU ministers, is regulation (EU) No 1252/2014 of May 2014.

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