At RAV Research we put a lot of focus and commitment in ensuring performance and quality of study deliverables. RAV Research implements the process, tools and metrics driven Site Support model which integrates all key drivers for the successful conduct of your studies at sites.

With our extensive experience, we understand that efficient and rapid start-up planning is key to the success of any clinical trial. We support the identification and selection of high quality and the most dependable investigator sites through our detailed and structured feasibility. RAV Research has agreements in place with many sites who have experienced investigators, suitable facilities and infrastructure as well as established processes for clinical trials.

We centrally organize and support simultaneous start-up activities for our sites through our team of experienced in-house project associates such as the collection of essential documents for the regulatory submission and drug release package, Informed Consent Form review and site specific customization of ICFs, Ethics Committee submission coordination, contract negotiation, adherence to local country specific requirements and addressing study specific needs at all the sites. This significantly reduces start-up timelines for RAV Research sites.

We deploy well-trained, qualified and dedicated site operations specialists and/or site coordinators at each Investigator site who provide support for the day to day study related activities at site and report centrally into our senior Project Managers at RAV Research.

In consultation with Investigators at site and with our client, RAV Research implements various metrics driven processes and tools such as quality indicators dashboard, error prevention plan, lessons learnt session etc. to ensure accelerated patient recruitment, proper study conduct and overall high quality and credible patient data at its sites.