Clinical development

Trusgen’s clinical development services encompass all the  services necessary to complete a cost-effective clinical trial.

Trial conduction strictly follows established Standard Operational Procedures (SOPs) or sponsor's SOPs per sponsor’s preference. Our Heads of Clinical Operations have more than a decade of experience in clinical trials.

· Phase I — IV clinical studies

· Phase I study protocol and CRF development

· Study conduct in healthy subjects and special populations

· Regulatory submissions and approvals

· Interim monitoring visits

· Data management

· Statistical analysis plans

· Statistical analysis of pharmacokinetic and pharmacodynamic data

· Statistical analysis of safety data

· Reporting

Our Services Include: