What is WHO-GMP Certification?
Good Manufacturing Practice ensures that products are consistently produced and controlled according to quality standards. WHO-GMP certification is often required for exporting pharmaceutical products.
It is granted after an inspection of the facility by the drug regulatory authority.
Who Needs WHO-GMP Certification?
- Pharmaceutical manufacturers
- Nutraceutical and cosmetic units
- Exporters to regulated markets
Advantages of WHO-GMP Certification
Export eligibility
Needed by many importing countries.
Quality assurance
Robust quality systems.
Documents Required for WHO-GMP Certification
Facility
- Manufacturing licence
- Site master file
- Standard operating procedures
- Validation and quality records
We share an exact checklist for your case after the consultation. Scanned copies or clear phone photos are fine.
How We Get It Done
- 1Gap assessment
Facility reviewed.
- 2Documentation
SOPs and site master file.
- 3Inspection
Regulatory inspection.
- 4Certificate
WHO-GMP granted.
Estimated timeline30–90 working days
Frequently Asked Questions
Generally 3 years, subject to inspections.