About this document
Regulatory Requirements for CROs in India by Neelam is a document available to read on EtoBox.
The document discusses regulatory requirements for contract research organizations (CROs) in India. CROs conduct clinical trials and other research services on behalf of pharmaceutical companies. The key regulatory body is the Central Drugs Standard Control Organization (CDSCO), which enforces safety and ethics standards. Pharmaceutical companies select CROs based on their ability to adhere to regulatory guidelines and timely complete trials. The India CRO market has grown in recent years due to lower costs
- Author
- Neelam
- Language
- EN