Meet Your Presenter
David R. Dills, an Independent Regulatory & Compliance Consultant, with an accomplished record and more than 20 years of hands-on experience, with emphasis on Class I/II/III medical devices, in vitro diagnostics, and pharmaceuticals in the areas of QA, regulatory affairs and compliance. Since 2000, he has provided consultative services on behalf of global manufacturers, subcontracted for third-party consultancies and provided services involving all key stages of the product development, submission and commercialization.
Mr. Dills has been previously affiliated with well-known device manufacturers and service providers, including a well-known CRO, and has served in various quality, regulatory and compliance management and advisory capacities with increasing responsibilities. Mr. Dills is an industry speaker and author of technical and compliance-related topics published in industry journals.
"David was very knowledgeable and presented the information in a clear and effective manner. He was very passionate about the subject,t making it a very enjoyable and exciting experience. His presentation was thoughtful and detailed. It put things in a whole new perspective for me. Great job!"
QA Associate, Bionique Testing Laboratories
"David was excellent! He brought serious applicable and pertinent industry examples that can really be applied."
Controlled Documentation Manager, Takeda Global, Research & Development
"David was very informative. Very well done – an excellent investment."
Technician, Musculoskeletal Transplant Foundation
"Great class, focused on how to write SOPs and the FDA's expectations."
Quality Manager, Sandvik Medical Solutions