Richard Reeve, President of RPR Consulting, has over 28 years experience in Clinical Quality Management and Clinical Operations in Pharma, Biotech and CROs in the EU and US. He has a proven track record of establishing and re-engineering GCP quality systems, and helping Sponsors prepare for and successfully complete regulatory inspections directed by FDA and EMA.

Combining a business-focused approach with practical operational experience he quickly identifies potential compliance issues and areas for optimization in your GCP system.