Linda K. Temple
Linda Temple has more than 25 years of experience in regulatory affairs and product development for drugs and medical devices. She worked at Beckman Coulter, Genzyme, Regulatory Affairs Professionals Society and Drug Information Association before founding her own company. Linda has led regulatory intelligence, technical training, and program development departments, and has also worked in clinical and research laboratories. She has published and presented extensively on regulatory affairs and related topics. She has degrees in biology, medical technology and business administration, and is RAC-certified.
Jessica J. Adams
Jessica Adams brings her Regulatory Project Management experience to her writing. She worked in Regulatory Affairs at Genentech, Cephalon, and AstraZeneca. Her projects covered drug development from the investigational (pre-IND filing) stage through the post-marketing stage. Jessica's educational background is as a medicinal chemist. In this role she has worked at DuPont, Guilford, and AstraZeneca. In addition, Jessica was a Regulatory Review Officer for the FDA's Division of Drug Marketing, Advertising and Communications, now called the Office of Prescription Drug Promotion.