Description

We provide thorough technical audits of pharmaceutical manufacturing facilities, evaluating key aspects such as infrastructure, existing machinery setup, and the potential for future expansion. Our audits include a detailed assessment of compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP), ensuring that the facility meets regulatory requirements and is capable of maintaining ongoing compliance. Additionally, we review record files, documentation, and past regulatory audit reports to identify any gaps in compliance. Based on our findings, we deliver a comprehensive GAP analysis report, highlighting areas for improvement and offering strategic recommendations for aligning with regulatory standards.