GMP Audits 

Good Manufacturing Practice, represents a set of stringent guidelines ensuring the integrity and transparency of manufacturing processes. In the pursuit of technological advancement, companies adhere to robust GMP standards to uphold fair and accountable practices throughout production cycles. Our organization conducts comprehensive audits aligned with GMP certification requirements and global quality standards. These audits cover a spectrum of materials and products, including Packaging Materials, API/Drug Substances, Excipients, Finished Products, Intermediates, Food Grade Materials, and Medical Devices.

GMP services, encompassing audits and compliance procedures, play a pivotal role across diverse industries. Among these services, GMP audits emerge as a cornerstone in regulatory affairs, encompassing various critical components:

• Supplier Risk Assessment
• Vendor Audit
• Supplier Qualification Process
• Due Diligence Audit
• Gap Audit/CSV Audit
• Pre-inspection Audit
• QMS Audit
• Independent Audit
• Root Cause Audit
• Data Integrity Audit
• EHS (Environment, Health, and Safety) Audit