Who We Are
International Clinical
Research Auditing Services
iCRAS is an independent third-party service provider specializing in delivering a wide range of GxP Auditing, Clinical Research SOP, Inspection Readiness and CAPA services proven to ensure our clients meet FDA and other global authority regulatory requirements. iCRAS partners with ex-FDA Auditors as well as with Certified Quality Auditors that have a minimum of 15 years of combined Clinical Research and Quality Assurance Field Auditing experience.
We specialize in conducting Good Clinical Practice (GCP) audits following the FDA BIMO program for the Medical Device, Biotech and Pharma industries to provide assurance that the data and reported results are credible and accurate. Globally experienced, we have conducted audits in the United States, Canada, Europe (East and West), China, Japan and Australia.