Sanjeevani is a professionally managed company with technocrat entrepreneurs at the helm of affairs. The clinical trials are conducted in compliance with ICH-GCP Guidelines, the approved protocol and regulated in accordance with the IRB and the Ethics Committee. Patient’s safety and well being is the core of our every day endeavour ensuring compliance with the highest regulatory, scientific & ethi
cal standards of ICH, WHO, USFDA, EMEA, MHRA, CDSCO
Sanjeevani offers Protocol and Case Report Form design, Monitoring, Report of serious Adverse Events, Data Management and Statistics, Development and implementation of Phase I-IV clinical trials, project management, contract development and negotiation, budgeting, study and site feasibility assessments, investigator selection, CRF development, study monitoring, monitoring reports revision, training, statistical analysis (SAS). Sanjeevani work with clients from all sectors of the pharmaceutical industry and help them maximize their research productivity and streamline drug development process. Our thorough understanding of the clinical and regulatory issues involved in clinical trials combined with our expertise in the outsourcing model made us one of the leading CRO in the market. Sanjeevani aims to be the best and foremost contract research organization committed to serve the pharmaceutical industry worldwide with high quality standards, at par with the international regulatory and professional expectations.
