SeerPharma provides expert GxP compliance support to pharmaceutical, medical device, and life sciences industries.
SeerPharma provides expert GxP compliance support to pharmaceutical, medical device, and life sciences industries.
Quality Management System (QMS) Implementation or Improvement –Robust systems that explain your specific business operations and address GxP regulatory requirements
GxP Compliance – Covering Manufacturing, Clinical, Laboratory, and Distribution
Facility Design & GMP Licensing – Ensuring compliance with TGA, EU & FDA regulations
Risk Management, Assessment & Compliance Strategies – Identifying, removing & mitigating risks
Validation Master Plans (VMP) – Strategy, oversight and execution of Validation activities
Process, Equipment & Analytical Method Validation – Meeting regulatory requirements
Computerised System Validation (CSV) – Ensuring compliance with PIC/S Annex 11 and 21 CFR Part 11 requirements
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