Clinical Trial Execution

TAB Clinical develops a plan unique to each sponsor based on their study needs.

• Site and Enrollment Plans
• IRB and Clinical Trial Agreement Plans
• Clinical Monitoring Plan
• Study Project Management
• Data Management Plan
• EDC, Statistics and Reports
• Lab Integrations
• Final Study Report Writing
• Drug Safety – Clinical
• Clinical Regulatory Documents
• Publication Planning – Manuscripts, Abstracts and Posters
• CSR Writing