ethica provides customized levels of support for Investigator-Initiated Trials (IIT). We can liaise with the Investigator, independently from the Sponsor or Granting Agency, to ensure a properly-constructed, ICH-GCP-compliant study protocol and the placement of necessary clinical trial logistics.

Without jeopardizing Investigator independence or OIG (Office of the Inspector General) compliance, ethica will ensure that the IIT is supported by highly-trained individuals with expertise to deliver non-confounding endpoints, outcome measures, data management and statistical methodology in the most timely manner.