These notes are intended to provide guidance on the recommended content of the SiteMaster File. A requirement for a Site Master File is referred to in Chapter 4 of the GMPGuide. INTRODUCTION1.1 The Site Master File is prepared by the pharmaceutical manufacturer and shouldcontain specific information about the quality management policies andactivities of the site, … Continue reading Preparation of a Site Master File as per MHRA →

Some useful guideline reference for Pharmaceutical industry but not limited to....

CQA : Corporate Quality assurance PV : Pharmacovigilance MK : Marketing QA : Quality assurance