by heaconwpadmin | May 17, 2025 | Pharmaceutical audits
the new EMA Q&A document dated 8 April 2025 (“Guidance on Good Manufacturing Practice and Good Distribution Practice: Questions and Answers”) makes direct reference to our business model and outlines specific expectations regarding the assessment of...
by heaconwpadmin | Sep 3, 2024 | Pharmaceutical audits
In spring 2024, the new VDI expert recommendation “3rd Party GMP Audits – Supplier Audits in the Pharmaceutical Industry” was published. The document provides a structured and professional method for evaluating and improving 3rd party audit...
