David LeProhon

David LeProhon

David LeProhon

Principal Consultant

David draws on 27 years of diverse experience in the Biopharmaceutical, Pharmaceutical, and Medical Device industries to assist companies in the development and compliance efforts to ensure robust quality programs, successful regulatory inspections, and maintenance of products, laboratories and facilities. 

David utilizes his broad background to assess compliance issues and develop effective, efficient, robust and comprehensive systems to ensure regulatory compliance. He assists companies in ensuring regulatory documentation is adequately implemented and maintained for quality systems, laboratory, and manufacturing operations.

Work Experience

Prior to joining Parexel, David held several management level positions, including an executive quality management role covering three global sites that manufactured combination (device/drug) products. He has extensive experience in validation, quality systems, regulatory inspections, method validation, vendor controls, and all aspects of pharmaceutical and medical device manufacturing. David has also worked in Development and Quality Control laboratories, API, drug product and Medical Device manufacturing facilities.


David holds a B.S. in Biochemistry from the University of Massachusetts and a M.B.A. from Southern New Hampshire University. He is a member of the Parenteral Drug Association and has presented several quality topics at conferences.

We are always available for a conversation.