What's involved in the clinical trial registration process
Once you register interest for a clinical trial with Evrima, you will be required to complete a series of steps which include Pre-Screening, Screening and Outcome.
- Pre-Screening - you will be required to complete a pre-screening survey and/or a phone call. The phone call will outline the study requirements, including the trial schedule, investigational treatment and location of the study site conducting the research.
- Screening - if it appears that the trial may be suitable to you, you will be referred to the study site where you will receive more detailed information and an informed consent form. You will have the chance to discuss the trial with the study doctor, ask any questions you may have, and consult your own GP (if desired) before signing the consent form.
- Outcome - should the study site conclude you are eligible to proceed with participation in the clinical trial, you will be enrolled onto the study, and your treatment periods will commence as scheduled with the study site.