Ensuring Manufacturing Quality, Safety & Compliance
Good Manufacturing Practice (GMP) verification by BQCIS assures that your production processes, control systems, and documentation meet sector-specific regulatory benchmarks. Whether in pharmaceuticals, food, cosmetics, or medical devices, GMP underpins product safety and market authorization.
We audit manufacturing facilities against recognized frameworks — including WHO GMP, PIC/S, EU GMP, and FDA cGMP — covering premises, process controls, cleaning validations, traceability, and change management. Our independent assessment ensures your systems maintain consistency, minimize contamination risk, and align with regulatory oversight.
Through GMP verification, clients can reduce product recalls, strengthen regulatory relationships, and gain confidence from stakeholders and consumers regarding production integrity.
Key Activities in GMP Verification
Key Benefits of GMP Verification
Regulatory Approval Confidence
Facilitates smoother audits and regulatory inspections across markets.
Enhanced Product Safety
Minimizes contamination and variability by verifying control systems.
Strengthened Customer Trust
Demonstrates your commitment to consistent, safe manufacturing standards.
Operational Efficiency Gains
Identifies process improvements and cost-saving opportunities via audit findings.
Success Story
GMP Verification for Nutraceutical Manufacturer
A nutraceutical producer needed to verify GMP compliance for international market access, with concerns over batch traceability and contamination control.
BQCIS conducted a full GMP audit, including facility inspection, process validation, lab controls, training protocols, and corrective action review aligned with WHO GMP and PIC/S standards.
The manufacturer achieved GMP verification in 10 weeks, enabling entry into EU and Asian markets and reducing batch rejection rate by 35%.