Clinical Trials Day

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

SANJEEVANI CLINICAL RESEARCH MANAGEMENT INCLUDES

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.