GMP — Good Manufacturing Practices
Good Manufacturing Practices certification for pharmaceutical, cosmetic, and food manufacturers — ensuring product quality, safety, and regulatory compliance throughout production.
Standard
WHO GMP Guidelines
Service type
By CAS
Issued under
CAS — own authority
What it is
Good Manufacturing Practices (GMP) are regulations and guidelines that provide minimum requirements for methods, facilities, and controls used in manufacturing, processing, and packing of products. GMP certification demonstrates a manufacturer's ability to consistently produce products that meet required quality standards.
Who needs it
Pharmaceutical manufacturers, cosmetics producers, nutraceutical companies, food manufacturers, and medical device manufacturers required to demonstrate GMP compliance for product registration and market access.
Benefits of certification
- Required for pharmaceutical product registration in Egypt and export markets
- Prerequisite for import licences in GCC, EU, and other regulated markets
- Demonstrates quality standards to regulatory authorities
- Reduces product quality failures, recalls, and regulatory actions
- Supports export to markets requiring WHO or EU GMP compliance
- Complements ISO 9001 and ISO 22000 certification
Frequently asked questions
Common questions
Is GMP the same as ISO 9001?
No. GMP is sector-specific (pharmaceutical/cosmetic) and required by regulators. ISO 9001 is a general quality management standard. Many organisations hold both — they complement each other well.
Which GMP standard applies to pharmaceuticals?
WHO GMP Guidelines are the most widely recognised globally. EU GMP (EudraLex Vol. 4) applies for EU export. CAS certifies against WHO GMP guidelines.
Ready to certify against WHO GMP Guidelines?
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