One of the most important tasks in the start-up of a clinical study is the submission to the ethics committees and the notification to relevant authorities.
We have extensive experience in the administrative and technical aspects of presenting studies, and obtaining Authorities and Ethics Committee approval. We have a regularly updated database of the procedures and information required for obtaining ethics approval.
Our excellent relationship with ECs has enabled us to help clients start their clinical trials rapidly.
- Investigator Recruitment
- Site Activation
- Clinical Trial Applications
- Project Launching and Planning Process