In Vivo provides a full range of clinical GCP audits from phase I to phase IV studies in Israel and on an international basis.
Clinical GCP Audits include all aspects of the clinical development process:
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Investigator Site Audits - Audits of studies involving single or multiple investigator sites on a worldwide basis.
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CRO and Clinical Laboratory Audits – Assessment (pre-contractual) audits or during ongoing projects.
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Trial Master File Audits - Inclusive review of essential documents according to ICH GCP, Local regulations and company’s SOPs.
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Phase 1 Unit Audits - Review of facilities, equipment, procedures and personnel, either pre-study or during study conduct.
