SynRG provides clinical trial services to pharmaceutical and bio-tech industry since 2002. Significant part of our experience was gained through participation in multinational mega-trials, which involved study start-up activities (site identification / selection, regulatory approvals, investigator meetings), clinical monitoring (site initiation, routine monitoring and closeout visits), site management, project management, safety reporting, handling of clinical trial materials, exportation of biological samples to the central lab, etc. A large number of our current trials come from repeat business.

SynRG conducts studies in all areas of medicine encompassing Cardiology, Infectious Diseases, Neurology, Oncology, Psychiatry, Rheumatology, and Vaccines, among the others.

We provide our clients with a wide range of Phase I-IV clinical trial services from protocol development to writing of final Clinical Study Report.

In addition to the core activities of a standard CRO, we also offer a wide spectrum of in-house and online training courses covering all aspects of clinical research. Our talented industry experts can help clients design and conduct studies in pharmacoeconomics using various analysis methods.