Supplementing the Directive regarding the principles and guidelines of good manufacturing practice for active substances used in medicinal products for human use
In the Official Journal of the European Union L 337 series was published the Delegated Regulation (EU) No. 1252/2014 of the Commission to supplement Directive 2001/83 / EC of the European Parliament and of the Council as regards the principles… Read moreSupplementing the Directive regarding the principles and guidelines of good manufacturing practice for active substances used in medicinal products for human use