Introduction
In pharmaceutical manufacturing, even the best systems and equipment are only as good as the people operating them. Personnel and training audits are essential to ensure that staff members are properly qualified, consistently trained, and fully compliant with regulatory expectations.
What Are Personnel & Training Audits?
These audits evaluate whether a supplier’s or vendor’s employees have the appropriate qualifications, skills, documentation, and ongoing training programs to carry out their roles in a GMP-compliant environment.
Key Areas Reviewed in a Training Audit
Why It Matters in Supplier Audits
apicule’s Role in Personnel Audits
At apicule, our audit team assesses vendor workforce readiness through detailed personnel file reviews, training matrix checks, and interviews with key roles. We identify gaps and recommend improvements to elevate workforce compliance and performance.
When developing analytical methods for pharmaceuticals, two critical aspects must be considered—validation and verification. While both ensure the accuracy and reliability of analytical techniques, they serve distinct purposes. Understanding their...
CMC (Chemistry, Manufacturing, and Controls) is one of the most critical components in any drug regulatory submission. It defines how a pharmaceutical product is developed, manufactured, and controlled to ensure...
IntroductionAn Abbreviated New Drug Application (ANDA) is the regulatory pathway for getting generic drugs approved by the U.S. FDA. Filing an ANDA is a strategic move that allows pharmaceutical companies...