Overview
Prime Pharma Partners leads CQV programs from construction completion through GMP readiness, integrating engineering, validation, automation, and quality into a single execution framework. We establish governance, control dependencies, and align cross-functional teams to ensure predictable, inspection-ready delivery.
Key Deliverables:
End-to-end CQV execution plans and integrated schedules.
Qualification protocols (IQ/OQ/PQ) aligned to execution strategy.
Risk registers, issue logs, and readiness tracking tools.
Inspection-ready validation and GMP evidence packages.
System turnover and closeout documentation
