GMP Certification (Good Manufacturing Practice)

GMP certification is granted to manufacturing or service systems of organizations to certify that they engage with good manufacturing practices in their manufacturing or service processes, according to a Standard Code of Practice related to their business.

Good manufacturing practice” or “GMP” is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices.

Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. 

GMPs – Good Manufacturing Practices have been used by the pharmaceutical and healthcare manufacturing industries for over 50 years as a means of assuring that products have the identity, strength, purity and quality that they purport to contain. GMPs are in effect in over 100 countries, and GMP compliance is a pre-requisite to exporting pharmaceuticals between countries. 

Benefits of GMP Certification

• Minimize the Food safety Hazards contamination in Food.
• Raw materials used in the manufacture of drugs are of known, and of possibly standardized, quality and are free from contamination; 
• The manufacturing process has been proven to produce a pharmaceutical product meeting its quality attributes; 
• Adequate quality control testing measures have been employed to assure that the product meets its quality specifications at time of release to market, and at the end of its shelf life. 
• GMP helps boost export opportunities.