Trial Site / Study Site

A Trial Site is the location where a clinical trial is conducted and/or coordinated, under the oversight of an Investigatorand 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)