A Trial Site is the location where a clinical trial is conducted and/or coordinated, under the oversight of an Investigator and in compliance with Good Clinical Practice (GCP) and regulatory guidelines. It can be a hospital, research institution, university, private clinic, or dedicated research facility where study participants receive investigational treatments and undergo study-related procedures.
The clinical trial site is responsible for:
- Recruiting and enrolling participants
- Administering the investigational product
- Collecting safety and efficacy data
- Ensuring adherence to trial protocols and regulatory requirements
- Reporting adverse events (AEs) and serious adverse events (SAEs)