More In-depth analysis of the requirements on the new EU / PIC/S Site Master File
More The number of Warning Letters issued to Drug Companies and API Manufacturers increases
More Quality of Herbal Medicinal Products - Current EMA/HMPC Q&A Document
More Results of the Survey "Implementation of the new Annex 1 requirements for Capping"
More New Pharma Directive on Counterfeit Medicine adopted by EU Parliament
More New version of EudraGMP allows access to information from all Member States
More EMA publishes ICH Q9 and ICH Q 10 as Part 3 of the EU GMP Guide
More Growing Requirements on Process and Technology Transfers
More EMA publishes two documents on the QP Declaration concerning GMP Compliance of the API
More PIC/S SMF Guide Updated with Quality Management System Requirements
More Detailed Analysis of FDA´s New Process Validation Guidance
More Clean Room Classification: Draft on ISO 14644 published
More News published about Guidance on Combating Counterfeit Drugs
More The New GMP Annex 11 and Chapter 4 is Europe's Answer to Part 11