Quality Assurance
Forza Pharma Consulting provides comprehensive Quality Assurance (QA) services to ensure compliance, consistency, and control across all phases of pharmaceutical and biopharmaceutical operations. Our QA professionals bring deep experience supporting GMP-regulated environments and external manufacturing networks, ensuring alignment with global regulatory requirements and Quality Agreements.
Areas of Expertise
Deviation investigation and root cause analysis (RCA)
Corrective and Preventive Action (CAPA) and effectiveness verification
Batch record and executed protocol review for completeness, traceability, and compliance
Change control review and risk assessment (Veeva, TrackWise, or equivalent systems)
Data integrity governance and 21 CFR Part 11 / Annex 11 compliance assessments
Quality oversight of Contract Manufacturing Organizations (CMOs) and service providers
QA support during manufacturing operations
Quality documentation, SOP development, and procedural gap assessments
Best Practices
Risk-based, phase-appropriate QA oversight tailored to project scope and regulatory expectations
Real-time QA presence to support right-first-time execution and reduce rework
Continuous improvement and inspection readiness through integrated QA-QC-CQV collaboration
Partner with Forza Pharma Consulting to strengthen your Quality Assurance programs and achieve sustainable GMP compliance.
