Gerry Buss

Mr. Buss has over 25 years of experience in the medical device industry directing quality and regulatory affairs programs for global companies, including over 20 years with GE Healthcare. His experience includes the introduction of various medical devices to the international market (FDA 510(k)s, EU Technical Files, and International Submission Dossiers), including medical ultrasound. He also has more than 20 years’ experience with cross-functional, international teams (direct and crisis, team building and support roles) and as a lead auditor (ISO9001, ISO13485, MDD, cGMP, CMDCAS).