GxP Audits
Comprehensive Good Manufacturing Practice (GMP) audits to ensure your facilities, systems, and processes meet global regulatory standards.
We offer specialized audits across different GxP domains:
- GMP Ensuring manufacturing facility meets strict quality and safety standards.
- GDP Ensuring warehouse and logistic facilities meets strict quality and safety standards.
- GLP Ensuring laboratory facility meets strict quality and safety standards
- GCP Audits (Good Clinical Practice) Ensuring clinical trials are conducted ethically and in compliance with regulatory standards.
- GPvP Audits (Good Pharmacovigilance Practice) Assessing pharmacovigilance systems for drug safety monitoring and reporting.
- Ready GMP Audit Reports Pre-prepared, industry-compliant audit reports designed to save time and streamline your compliance processes.
- Formulated medicinal products; sterile/non-sterile
- API / API intermediates; sterile/non-sterile
- Fermentation-based APIs, Biological formulation products
- Raw materials (API, Excipients, Key Starting Materials (KSMs)
- Packaging materials
- Distributors, warehouses, GDP
- Contract testing Laboratories
- Medical devices
