“The success of any project depends on lining up the right resources, in the right combination, at precisely the right time”. iVRS delivers the competencies, resources and systems essential to cover every aspect of the drug development process. Our dedicated scientists, clinicians, investigators, regulatory experts are committed to highest quality of ethical standards. We provide services that would challenge assumptions about traditional clinical trial design and management so that credible, clean clinical data is obtained within budget, on time, every time.

Throughout the duration of the trial, iVRS offers the singular focus of a dedicated team for consistent effective interaction with study sites. The project manager, fully supported by iVRS, is responsible for seamless communications with your organization. Rigorous ongoing training for project teams in drug and disease management and compliance as well as protocolspecific practices assure you of a monitoring team with the clinical know-how to get quality results that meet timelines. 

We follow a rigorous scientific approach to the “art” of staffing, troubleshooting and risk management. Resource charts are prepared to facilitate the exact number of people in each speciality needed during each phase of the project. We develop critical path analysis that flags activities with dependencies. Based on past experience, we bring formidable analytical skills to minimize all possible risks. As your research partner through the critical phases, iVRS helps you develop strategies to:

◘ Recruit the right patients

◘ Conduct the study within estimated costs

◘ Ensure National, International quality and regulatory compliance