White Papers related to Quality Systems and Compliance
White Paper
- January 10, 2022
Legal and regulatory requirements, including GMP and GDP guidelines, require consistently that medicinal products shall be stored and transported in a way that the product delivered maintain their quality and integrity and remain within the legal supply chain during storage and/or transportation. Storage and transport need to be described in the Pharmaceutical Quality System and the principles of quality risk management shall be used for designing and managing these activities.
White Paper
- July 12, 2021
Download our recent whitepaper to gain deep insights into the Monitoring Compliance with Safety Exchange Agreements.
White Paper
- July 7, 2021
Download our recent whitepaper to gain deep insights into the mutual recognition of inspections of medicinal product manufacturers between the EU and the USA.