2. Our Vision:- We; Jupiter Research Services; are a Clinical Research Service provider, providing the core clinical research services like site management, clinical trial management, site feasibility, site start up, etc. Our sole purpose is to support the successful outcome of clinical trials for the pharmaceutical, biotechnology, and medical device industries. Our goal is to earn the recognition as a company that provides our customers with unparalleled service, responsiveness, and results. We continually strive to be the finest resource for you and to ensure that we satisfy your specific and unique needs.

3. What services we do provide? To the companies and organizations conducting clinical trials… Investigators and study sites with enough strength and commitment to conduct a clinical trial. Jupiter assures and guarantee the best service in terms of trial conduct in compliance with GCP guidelines and most credible & reliable data. To the sites and investigators… Experienced and dedicated Clinical Research Coordinators assisting the physicians in the preparation and conducting of these trials.

4. How do we conduct our business? We conduct our business within the Code of Ethics. In best compliance with the ICH-GCP guidelines, FDA regulations, Nuremberg code, Declaration of Helsinki ICMR guidelines and Schedule Y.

5. What We do have??? We do have educated, qualified, experienced, pre- screened, Principal Investigators, clinical research coordinators, clinical research associates for conduct of clinical trials in any clinical specialities. This includes single practitioners, large single and multi-specialty practices, physician networks, hospital based physicians, etc.

6. Contd.. The Investigators linked with the JUPITER network are evaluated to ensure they not only are qualified to conduct clinical trials, but have the patient population and administrative capabilities to properly conduct it. They must meet specific minimal standards before being included in the network. We only present those Investigators meeting the specific selection criteria outlined by the Sponsor or CRO. This eliminates a significant amount of time and expense when attempting to qualify, enroll, and initiate a site.

7. We ensure timely and accurate regulatory board submission and data collection… All sites will have Dedicated, Full time, and Experienced Clinical Research Coordinators to ensure the, Prioritized and Accurate Regulatory Submissions, Appropriate Site Initiation, Patient screening, recruitment, and enrollment Generation, collection and management of clean, credible, reliable and accurate data.

8. Quality check and assurance from our side… Our own internal management and quality assurance practices further assures that tasks are completed quickly and accurately and any problems that jeopardize the success of the study are quickly identified and resolved.

9. For further details and queries free feel to contact: Jupiter Research Services C/o Mr Pratik A. Shah 09429605962 (M) Email: Jupiter.crs@gmail.com pashah8288@gmail.com