GMP — Good Manufacturing Practices
Good Manufacturing Practices certification for pharmaceutical, cosmetic, and food manufacturers — ensuring product quality, safety, and regulatory compliance throughout production.
This certificate is issued by CAS without third-party accreditation for this scheme. It is not within the scope of EGAC Schedule 012418B and is not recognised under the IAF MLA. Per IAF MD 23:2023, CAS clearly differentiates accredited and non-accredited services on every page.
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.
Pharmaceutical manufacturers, cosmetics producers, nutraceutical companies, food manufacturers, and medical device manufacturers required to demonstrate GMP compliance for product registration and market access.
- 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