WHO defines Good Manufacturing Practices (GMP) as "that part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization."

WHO GMP is part and parcel of quality system that encompasses manufacturing and testing of active food ingredients, pharmaceutical ingredients and products, medical devices, diagnostics, and medical devices. GMP Certification confirms the products’ identity, composition, quality, purity and strength which they represent in the market. Under it, there is a set of guidelines that offer a system of procedures and documentation by which the confirmation of the products are given. We offer consultancy on attaining GMP Certification that will give your product a high boost in the market.

• WHO GMP covers all aspects of the manufacturing process including :

• Defined manufacturing process

• Validated critical manufacturing steps

• Suitable premises, storage, transport, qualified and trained production and quality control personnel

• Adequate laboratory facilities

• Approved written procedures and instructions

• Records to show all steps of defined procedures have been taken

• Full traceability of a product through batch records and distribution records

• Systems for recall and investigation of complaints

• Reduced duplication of inspections

• Enhanced market access

• Export facilitation

• Cost savings

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