- BA/BE Study of Drugs as per the Regulatory guidelines of the Particular country Specified by the Sponsor.
- Clinical site management as per requirement by the sponsor.
- Clinical Trial of Phase II, III and IV for Synthetic Drugs and Herbal Drugs as per schedule Y, ICMR and ICH-GCP guidelines
- Preparation of Clinical trial Protocol for Synthetic Drug and as well
as Herbal Drug and Regulatory Approval there of
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