Business Development for the Sites and Its Capabilities

• Getting the most interesting projects for you
• Assist in building a research set-up at your site

Pre-Study Site Preparation

• Feasibility Study
• Trial Budgeting
• CTA Review
• Collection Of Essential Documents
• CRF
• ICF

Site Initiation & Training

• Streamlined And Expeditious Site Start-Up
• Staffing-Trained And Experienced CRCs
• ICH-GCP Training And Protocol Specific Training
• Patient Recruitment Strategies And Follow-Up
• IP Management
• Lab Handling Procedures
• Logistics Management
• Site Specific SOPs
• Interacting With Regulatory Agencies
• Monitoring And Audits/Site QA
• EC Approval
• Archival Of Site Documents
• Maintain And Update Site Master File
• Timely Resolution Of Queries
• Adverse Event Reporting

Study Close-Out

• IP Accountability
• Availability Of All Study Documents
• Resolution Of Study Related Issues

For Doctors

• Assistance In Investigator-Initiated Trials
• Data Management
• Article Writing