Nov. 28 – Validation Documentation Requirements and Responsibilities for Drug Fabricators, Packagers / Labellers, Testers, Distributors and Importers
A new version of the document entitled “Validation Documentation Requirements and Responsibilities for Drug Fabricators, Packagers / Labellers, Testers, Distributors and Importers” is now available. This document has been reviewed as part of the Inspectorate’s quality management process and has been amended to further clarify issues brought to the attention of the Inspectorate.
