Philippe B.

Philippe B. has extensive experience in regulatory affairs, quality assurance, and clinical affairs. Philippe started their career in 1992 as a Manager of Regulatory Affairs at 3M Health Care, where they worked until 1997. During their time at 3M, Philippe managed regulatory activities and developed regulatory strategies.

In 1997, Philippe joined Datascope as the Director of Regulatory and Clinical Affairs and Quality Assurance. Their responsibilities at Datascope included managing all regulatory activities globally, including product submission and approval for life supporting devices. Philippe also oversaw quality assurance and control activities, including product releases and non-conforming product review.

Philippe then moved to MaQuet CardioVascular in 2009, where they held the position of Director of Regulatory & Clinical Affairs and Quality Assurance. In this role, they managed regulatory and clinical affairs as well as quality assurance. Philippe worked at MaQuet until 2011.

Finally, Philippe joined Collplant in 2011 as the VP of Regulatory Affairs and Quality Assurance. In this role, they continue to oversee regulatory affairs and quality assurance for the company.

Philippe B.'s education history includes an unspecified PharmD program from an undisclosed institution, without any specific start or end years mentioned. No details regarding the degree name or field of study are provided.