European Commission Consults on Revised GMPs for Sterile Drugs
By Michael Mezher -
Published 20 December 2017
The European Commission on Wednesday launched a three-month public consultation ahead of its planned revision to good manufacturing practice (GMP) rules for sterile medicinal products contained in Annex 1 of Eudralex Volume 4.
Categories: News, Europe, EC, Drugs, Manufacturing
Tags: Eudralex Volume 4, Annex 1, Sterile Drugs, Good Manufacturing Practice, GMP