First Steps to Upgrading Pharmaceutical Manufacturing

Whether building a new facility (greenfield) or upgrading a pharmaceutical manufacturing site (brownfield), it is important to understand the regulations governing facilities and inspection readiness. The Code of Federal Regulations Part 211 governs the United States, Eudralex Volume 4 governs the European Union, and the Ministry of Health, Labour, and Welfare govern Japan.   GMP … Continue reading First Steps to Upgrading Pharmaceutical Manufacturing