ZOOM finds, initiates, and manages clinical trial sites in India

All site level operations assured by standardized SOPs

• Development, Review and Approval of Standard Operating Procedures
• Feasibility Assessment
• Organizing a Site for Clinical Research
• Ethics Committee Communications
• Subject Screening and Recruitment
• Site Master File
• Informed Consent Process
• Management of AE's and SAE's
• Completing Case Report Forms
• Dealing with Deviations and Violations
• Management of Data and Source Documents
• Preparation for Monitoring Visits
• Subject Follow up
• Study Closure
• Preparations for Audits/Inspections
• Investigator Source Document Verification Agreement
• Handling Investigational Products
• Patient Flow
• Roles and Responsibilities of the Research Team
• Scanning Source Documents
• Management of Biological Specimens, Collection and Storage

ZOOM minimizes LTFU and Protocol Violation cases due to close care and subject follow-up

ZOOM employs the latest Internet, Print and Scan technologies to enable highly efficient trial conduct

ZOOM will soon be offering Source Documents Online saving monitoring $$$ and time