From site qualification to closeout visits
We offer our thorough knowledge and ability to apply all relevant regulations, together with our vast clinical experience; this allows us to effectively interact with sites with optimal results and excellent timing.
- selection of site and investigators
- documented monitoring visits, clinical and technical support to sites, applying all international and national regulations
- competent and complete SD verification, supported by sound clinical knowledge and permanent education
- continuous and planned contacts with sites, for constant updating on every aspect during the course of clinical trial
- tailored newsletters
- detailed identification, reporting, follow-up and reconciliation of AEs
- COVs completed with support for correct filing at site and reconciliation of study medication accountability
- services tailored on specific sponsor, study and site requirements