FULL RANGE OF SERVICES

Sanjeevani offers a full range of clinical research services for the pharmaceutical, medical device, biopharmaceutical, and CRO industries including:

	Study Development
	Protocol Development
	CRF Design & Distribution
	Site Management: Solicitation, Qualification & Selection
	Patient Recruitment
	Regulatory Management
	Project Management
	Study Monitoring
	Medical Monitoring/SAE Reporting
	Statistical Analysis, Programming & Reporting
	Pharmacovigilance
	Data & Report Management
	Data Verification and Validation
	MedDRA & WHO Drug Coding
	Risk Management
	Comprehensive Medical Report Writing

	Managing a comprehensive portfolio of grants, cooperative agreements, and contracts to implement in all aspects of clinical research trials.
	Helping site staff understand their responsibilities for ensuring that the research is of high quality and conducted in accordance with all applicable regulations and Guidelines.
	Developing procedures for the management of clinical sites.
	Providing each clinical trials program with resources for developing study Protocols, coordinating program-wide communication, and monitoring the performance of individual sites and the program as a whole; and identifying factors negatively affecting program performance and addressing these problems in collaboration with the program’s leadership.

Services