GMP stands for Good Manufacturing Practice, and the word is used globally to manage the control and management of pharmaceutical product manufacturing, testing, and overall quality. It establishes certain rules for the quality assurance approach. GMP accreditation ensures that items are manufactured in accordance with quality standards.
The Commissioner of the Food and Drug Administration has authorised the Joint Commissioner to sign and issue certifications under the WHO-GMP certification programme. Documentation, record keeping, employee qualifications, sanitation, cleanliness, equipment verification, sanitation, complaint handling, and process validation are all covered by GMP certification.
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