Robert M. Di TullioVP, Regulatory Affairs, Quality, & Clinical Affairs
 Robert M. Di Tullio joined Sequenom as Vice President, Regulatory Affairs, Quality and Clinical Affairs in June 2007, bringing more than 30 years experience in the in vitro diagnostics industry. Most recently, he was Vice President, Global Regulatory Affairs at Siemens Medical Solutions Diagnostics. He joined Siemens following that company’s acquisition of Diagnostic Products Corporation (DPC), where he served as Corporate Officer and Vice President, Regulatory Affairs, Clinical and Quality Systems. He joined DPC from his prior employment at Cirrus Diagnostics, when DPC acquired Cirrus in 1992. He previously held regulatory and quality leadership positions with Pharmacia and Behring. Robert is currently the co-chair of the AdvaMed Diagnostics Task Force, was an advisory board member for the Medical Device graduate degree curriculum at the University of Southern California for several years and has numerous professional regulatory affairs society affiliations.
He received a B.S. in Biology from Saint Joseph’s University in Philadelphia. |