Learn about the process for ensuring controlled storage conditions, temperature mapping. Discover key equipment considerations. cGMP Consulting can help!
Learn why temperature mapping is vital for FDA-regulated distributors—ensuring compliance, product integrity, and risk protection.
Learn about Commissioning, Qualification, and Validation (CQV) in cGMP environments to ensure compliance and product quality in the pharmaceutical industry.
Explore the Factory of the Future with Shivani Upadhyay’s guide. Learn about digital technologies, agile processes, and modular tech to transform your manufacturing.
Discover what a Periodic Validation Review (PVR) is, how it's conducted, and how often it should be performed to ensure ongoing compliance and system control.
cGMP Consulting has helped clients stay compliant with the current Good Manufacturing Practices (cGMP) and implement new technologies since 2001.
We are ISO accredited to perform GMP Certification Audits.
© Copyright 2001 – cGMP Consulting Inc. All Rights Reserved | Privacy Policy