The growth of
the clinical research market in India—specifically, the growth
of CROs has been phenomenal. The professionals working in Site Management
Organizations (SMO’s) have played a pivotal role in helping
the country deal with this rapid growth and ensuring that clinical
research is being conducted following ICH-GCP and India-GCP standards.
This is especially important in emerging markets such as India,
where there are many investigators conducting clinical trials for
the first time. The emergence of SMOs in India has helped to alleviate
this concern by assisting investigators with day-to-day study conduct
activities, ensuring that investigators are following the protocol,
interacting with ethics committees, and helping to provide high-quality
data from sites. In fact, the vast majority of trial data that has
been accepted by the FDA for Indian trials has come from studies
involving SMOs.
- Post Graduation Certificate in Clinical Reserch
- Fees: Rs.60,000
- Duration: 6 Months
- Starting Date: 3-09-2010
- Centre: Goa
- Post Graduation Diploma in Business Administration in specialization with Clinical Research and Pharmaceutical/Healthcare Management ( PGDBA)
- Fees: Rs.50,000 Per Semester
- Duration: Two Semesters
- Starting Date: 3-09-2010
- Centre: Goa
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