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Swapnil Fernandes

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MARKETING AUTHORISATION, LICENSING AND QUALITY ASSESSMENT OF VACCINES IN INDIA, US AND EUROPEAN UNION.
Common Technical Document (CTD)
FSSAI REGULATIONS FOR THE IMPORT, MANUFACTURE AND SALE OF NUTRACEUTICALS IN INDIA, RECOMMENDED DIETARY ALLOWANCE (RDA)
Current Good Manufacturing Practices
Quality System Requirements 21 CFR Part 820 and Labelling Requirements for Medical Devices 21 CFR Part 801
Code of Federal Regulations
The Pharmacy act, 1948
Good Automated Laboratory Practices