ethica CRO


Clinical
Study Management
Investigator Initiated Trials

ethica CRO provides customized support for Investigator-Initiated Trials (IITs). We can liaise with the Investigator, independently from the Sponsor or Granting Agency, to ensure that a properly-constructed, ICH-GCP-compliant study protocol is developed, and that all necessary clinical trial logistics are put in place.

ethica CRO ensures that the IIT is supported by highly-trained individuals with expertise to ensure proper study conduct, respect of timelines and deliverables, appropriate data management processes and statistical reporting. Importantly, this support is delivered without jeopardizing Investigator independence or OIG (Office of the Inspector General) compliance.

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ethica Investigator Manual