Concept Paper on the revision of Annex 11 of the guidelines on Good Manufacturing Practice for medicinal products – Computerised Systems
Title:
Concept Paper on the revision of Annex 11 of the
guidelines on Good Manufacturing Practice for medicinal
products – Computerised Systems
Origin/Publisher:
European Medicines Agency
Content:
This concept paper addresses the need to update Annex 11, Computerised Systems, of the Good Manufacturing Practice (GMP) guide. Annex 11 is common to the member states of the European Union (EU)/European Economic Area (EEA) as well as to the participating authorities of the Pharmaceutical Inspection Co-operation Scheme (PIC/S).