GMP addresses issues including documentation, record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open ended, allowing each manufacturer to decide individually how to best implement the necessary controls.
GMP Certificate is part of an organization’s quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, cosmetics, pharmaceutical products, and medical devices till it reaches the point of use.
To know more about GMP Certification and other standards, please visit our website.
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