Compliance Auditing: A Peek Into Common Critical Findings

Compliance auditing is an essential process in the pharmaceutical industry, serving as a safeguard to ensure that pharmaceutical products and medical devices meet stringent standards of safety, effectiveness, and quality. This process involves a thorough, systematic evaluation to verify that a firm adheres to all relevant regulatory requirements, industry standards, and maintains robust internal policies and procedures.

The significance of compliance auditing cannot be overstated, as it is fundamental to protecting public health and ensuring that products on the market are safe for consumer use. In this article, we delve into common critical audit findings identified by global health authorities and examine the key observations made by ProPharma’s GxP Compliance Auditors based on their extensive experience. Understanding these insights is crucial for firms aiming to uphold the highest standards of quality and regulatory compliance.