Clinical Research & GCP Specialist
Robert FannonMBA
All phases of pharmaceutical and device clinical trials, with mock-FDA audits across GCP, GXP and GLP and extensive international audit experience.
- GCP
- GLP
- Clinical Trials
- Gap Assessment
- International Audits
30+ years industry
Background
Robert Fannon has more than 30 years of industry experience across all phases of clinical trials for both pharmaceuticals and medical devices. He performs mock-FDA audits in GCP, GXP and GLP areas, conducts GMP gap assessments, and has expertise in project management.
He has participated in numerous remediation activities helping firms achieve compliance with clinical research federal requirements as well as Good Manufacturing Practices, and has extensive experience conducting both international and domestic audits.
He has published in Thrombosis Research 42, p789-796, 1988.
What Robert does on an engagement
- GCP, GXP and GLP mock-FDA audits
- Clinical research remediation programs
- GMP gap assessments
- International and domestic audit programs
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