About GMP Certification (Pharmaceutical & Food)
GMP (Good Manufacturing Practice) certification verifies that manufacturing processes and facilities consistently produce products of the quality required for their intended use and as required by the product specification. GMP certification is mandatory for pharmaceutical manufacturers and increasingly required in food manufacturing across Asia.
Our GMP Certification (Pharmaceutical & Food) Services
- WHO GMP for pharmaceutical manufacturers
- EU GMP compliance (for export to European markets)
- ICH Q10 Pharmaceutical Quality System implementation
- GMP gap analysis and remediation support
- Mock GMP inspection preparation
- GMP documentation and SOP development
- US FDA cGMP (current Good Manufacturing Practice) compliance
- Schedule M GMP compliance (India) for pharmaceutical manufacturers
Why Work With ISOAsia?
ISOAsia has guided hundreds of Asian businesses through GMP Certification (Pharmaceutical & Food) and related compliance programmes. Our consultants combine deep regulatory knowledge with practical implementation experience โ ensuring your certification project is completed efficiently, correctly, and to the highest standard.
Free Initial Consultation: Not sure if GMP Certification (Pharmaceutical & Food) is right for your product or business? WhatsApp our specialists for a free, no-obligation assessment of your requirements.
Frequently Asked Questions
WHO GMP guidelines are the Good Manufacturing Practice guidelines published by the World Health Organisation. Many Asian drug regulatory authorities (including in India, Vietnam, Malaysia, and Indonesia) use WHO GMP as the basis for pharmaceutical manufacturing compliance requirements.
GMP is a broader concept covering pharmaceuticals and food. ISO 22716 is GMP specifically for cosmetics. Pharmaceutical GMP is covered by WHO GMP, EU GMP, and US FDA cGMP guidelines, which go beyond ISO standards.