- +91-821-983-3540
- 01762-503026
- info@pharmaffairs.in
External Audits
- Perform Technical Audit of pharmaceutical manufacturing facility: including assessment of infrastructure, existing machineries setup, and its expansion capabilities.
- Assess compliance with GMP, GLP by checking the manufacturing facility and its capability for further regulatory compliance.
- Look into the record files and their documentation as well as any past regulatory audit and compliance report.
- Draft a report on the GAP analysis.
