What are the most common findings in a GMP audit?
Good Manufacturing Practice (GMP) is a system of standards and guidelines that ensure the quality, safety, and efficacy of pharmaceutical, biotechnology, and medical device products. GMP audits are inspections conducted by regulatory authorities or third-party auditors to verify the compliance of manufacturers and suppliers with GMP requirements. A GMP audit can reveal strengths and weaknesses in the GMP quality system and identify areas for improvement or corrective actions. In this article, we will discuss some of the most common findings in a GMP audit and how to avoid them.