GMP GOOD MANUFACTURING PRACTICES CERTIFICATION

How Do I Get a GMP Good Manufacturing Practices Certificate?
• Receiving the application and signing the contract (FR-SP-02 Certification Agreement),
• Planning the audit (PRS-11 audit planning procedure),
• Performing the audit (PRS-05 system certification procedure),
Certification Committee Decision,
• Publishing the Document.

GMP (Good Manufacturing Practices) (Good Manufacturing Practices)
It is a set of requirements developed and implemented by the FDA to produce products such as medicines, cosmetics, food, medical and in-vitro devices that directly affect human health under reliable conditions.

Good Manufacturing Practices (GMP) has been adopted by the American Food and Drug Administration (FDA) as a health and food quality standard that covers the mandatory rules from the production stage to the delivery of all kinds of products and services.  In time, it has been put into practice adopted by the World Health Organization and other countries.

GMP applications have been made compulsory in many areas in our country and are demanded as the basic requirement in workplace licences.

The ISO 22716 standard was published by ISO (International Organization for Standardization) in 2007 for applications specific to the cosmetic industry of GMP applications.

GMP Benefits
Compliance with legal requirements,
International validity,
Superiority in the market,
Traceability,
Continuous improvement.

Certificate Validity Period: 3 Years
Audit Period: At least every 12 months.