Пересмотр Руководства по GMP EC – Приложение 16
- 18 октября 2015
On 12 October 2015, the European Commission published revised version of Annex 16: Certification by a Qualified Person and Batch Release of the EU GMP Guide. The new annex will become effective on 15 April 2016. General principles Revised version of the annex states that: The ultimate responsibility for the performance of a medicinal product over its
