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