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DCGI to implement e-Gov in its working The Drugs Controller General of India (DCGI) to have a single window facility for drug approval soon...
New Indian Regulatory Guidance by Central Drugs Standard Control Organization Guidance for Industry on Submission of Clinical Trial Application for Evaluating Safety and Efficacy - Central Drugs Standard Control Organization...
Indian Clinical Data Management market is expected to ramp up to $150 million MNCs are more than willing to outsource their needs to India because of it\'s technological innovation, creditable quality, operational flexibility, cost effectiveness, time-to-market and competitive advantage according to Koteshwar Govind, Deputy Manager,...
India: Attractive Market for Biopharmaceutical Companies Looking to Accelerate Their Clinical Trials The Clinical Research Market in India is growing at a very rapid rate according to anyone’s statistics…It is exploding according to all the hype. ...

Site Management » Site Feasibility & Site Selection


Study Feasibility is conducted to select the best investigators and site

The feasibility for any protocol and therapeutic indication is done across India and the feasibility report is generated which includes:

* Epidemiological background of the disease – its incidence & prevalence rate.
* Disease & its Clinical presentation in India.
* India specific disease mortality and morbidity rate.

Standard of Care in India: o Hospital facilities & Medical care in India.
o Treatment protocol
o Lab facilities including CAP/NABL accredited Central Lab
o Facilities for Imaging / Radiological investigations.