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Documents CDSCO-GuidanceForIndustry


 Guidance for Industry • Submission of Clinical Trial Application for Evaluating Safety and Efficacy • Requirements for permission of New Drugs Approval • Post approval…

Documents Gmp

INTERNATIONAL AGREEMENTS GOOD MANUFACTURING PRACTICES Quality of all drugs is essentially the responsibility of manufacturers and it has assumed significant importance in…

Documents CDSCO-GuidanceForIndustry


 Guidance for Industry • Submission of Clinical Trial Application for Evaluating Safety and Efficacy • Requirements for permission of New Drugs Approval • Post approval…