|
|
Clinical Research
Regulatory Affairs
We understand that time is money , so our aim is to assist you with a broad range of regulatory affairs services that can help you in successful submission at the shortest time possible for all the phases of the drug development and approval process from Drugs Controller General India, Directorate General of Foreign Trade, and Indian Council of Medical Research
- Regulatory strategy
- Preparation and submission of complete range of regulatory documents for obtaining
- Approval to conduct clinical trial in India
- Approval to import Test Drug
- Approval to export Biological Samples
- Safety Reporting
|
