Insight's Clinical Trial team is uniquely positioned to partner with you within your timeline and budget for your clinical trial needs. From early proof of concept to planning, developing, setting up, and coordinating day-to-day management of contracted clinical trial protocols and their execution in accordance with regulatory agency rules and standards, to the last phase of clinical trials and delivering quality work in a timely fashion. We follow the ICH Clinical Practice (GCP) and the regulatory guidelines set by the country where we conduct the clinical trials.

Our wide range of services regarding clinical trials include but is not limited to:

• Identification, Selection, and Management of Clinical Sites
• Clinical Site Oversight
• Patient Pools and Enrollment
• Phase I-IV Protocol Development
• Patient Education Materials
• Safety and Efficacy Reporting
• Quality Oversight and Control
• Record Management Plan
• Compliance Reports
• Phase I-IV Protocol Development
• Phase I-IV Clinical Statistics Reports
• Phase I-IV Clinical Study Reports
• Project Management (Project planning, Risk Management, Budget, Timeline)