Debe Deck is a regulatory affairs professional specializing in both FDA and international regulatory affairs. With over 25 years of experience, she held positions at Chiron Vision and during her long tenure at ClinReg Consulting Services, helped clients gain worldwide approvals for a wide range of medical devices in the U.S., EU, Canada, Australia, Latin America, South Africa, and Pacific Rim countries. Ms. Deck has served as a regulatory project manager for multiple novel Class 3 technologies, including original IDEs and PMAs. She has extensive experience leading teams through the development of strategic product submissions including IDEs, 510(k)s and PMAs for capital equipment including ophthalmic lasers and permanent implants.
Regulatory Pathways Group Inc.
a California corporation
Inquiries and general information:
info@regulatorypathways.com