Selecting and supporting study sites to maximise trial outcomes
A key factor to a study’s success is the investigational site, and so too is the way it is managed.
We match the needs of your study with the ideal location through our extensive database of site investigators, resources and personnel that span many international locations. A dedicated site manager works closely with sponsors to develop patient recruitment strategies and maintain the site in accordance with the International Conference on Harmonisation Good Clinical Practice (ICH GCP).
- Study feasibility assessment and identification of key site requirements
- Global Investigator Site Identification and Evaluation
- Efficient site start up support
- Proactive Contract and Budget negotiations
- Comprehensive site qualification and support
How we work
Experienced investigators
Accelagen works with subject matter experts who add value to your study through specialised insight of your therapeutic area.
Access to target patient populations
Our wide network of trial sites help you find the right participants for your research, within your budget and timeline.
Best practice site management
Upholding compliance with robust quality management, documentation and procedures.
Site identification and management
case studies
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