What is WHO-GMP?
WHO-GMP (World Health Organization Good Manufacturing Practices) is the international benchmark for ensuring pharmaceutical products are consistently produced and controlled to quality standards.
Think of WHO-GMP as a detailed "recipe and kitchen protocol" for medicine, ensuring the right ingredients are used in the right way, with complete traceability and quality control.
Quality Assurance
Every batch tested and verified
Complete Documentation
Full traceability of all processes
Trained Personnel
Qualified staff at every stage
Benefits of WHO-GMP
Why UK pharmaceutical companies need WHO-GMP certification
Export Markets
Access emerging markets in Africa, Asia, and South America that require WHO-GMP certification.
UN/NGO Tenders
Qualify for WHO prequalification and supply to UN agencies and international NGOs.
Patient Safety
Ensure medicines are safe, effective, and consistently meet quality specifications.
Customer Trust
Build credibility with international buyers and regulatory authorities.
Process Control
Systematic approach to manufacturing reduces errors and batch failures.
MHRA Alignment
Complements UK domestic GMP requirements for comprehensive compliance.
Who Needs WHO-GMP?
Essential for UK pharmaceutical exporters
Finished Dosage
Tablets, capsules, injectables
API Manufacturers
Active pharmaceutical ingredients
Herbal Medicines
Traditional herbal products
Contract Mfg
CMO/CDMO services
Certification Process
Your path to WHO-GMP certification
Gap Assessment
Evaluate current systems against WHO-GMP requirements
System Development
Develop PQMS documentation, SOPs, and validation protocols
Implementation
Roll out systems with staff training and qualification
Regulatory Audit
Inspection by MHRA or national regulatory authority
Ready to Export Globally?
Get WHO-GMP certified and access international pharmaceutical markets.