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.

1. Post Graduation Certificate in Clinical Reserch
   • Fees: Rs.60,000
   • Duration: 6 Months
   • Starting Date: 3-09-2010
   • Centre: Goa


2. 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