Richard G. Jones
Senior Vice President, Clinical and Regulatory Affairs, and Quality Assurance
For more than 35 years, Senior Vice President, Clinical and Regulatory Affairs, and Quality Assurance, Richard G. Jones has represented the regulatory interests of the pharmaceutical and medical device industries, among others.
He has worked for both large and small medical device companies, acquiring vast experience in FDA regulation compliance, new product approval submissions, international experience for ISO Certification, CE Certification, and Canada Marketing Approvals. His clients have included Glaxo Smith Kline; Johnson & Johnson, Surgikos; Teleflex, Pilling Weck; Surgical Laser Technologies (Photomedex); American Medical Products; and Surgical Specialties Corporation.
His experience, along with his formal training in biology, microbiology and pharmacology, equips him to identify the direction and new product investigations to obtain FDA approvals in bench testing, animal testing, shelf life studies, sterilization and clinical studies. He has represented wide range of products, including hemodialysis/intraperitoneal dialysis devices, hydrocephalus shunts, cardiovascular catheters, surgical drapes and gowns, vascular grafts, absorbable hemostatic sponges, I.V. infusion pumps, electro-stimulation devices, surgical instruments (reusable/disposable), contact lasers, microsurgical sutures, and ophthalmic devices.
Mr. Jones’ philosophical approach is based on collaboration with the regulatory agencies to establish the scientific requirements for new product approvals in minimal time in the most cost-effective program.
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