Medical Device Services Director
Celegence
Joy has 30+ years’ experience working in the medical device manufacturing industry as a Regulatory Affairs Professional. Key experience includes MDD/MDR compliance, developing/maintaining technical files and design dossiers, international marketing authorizations, risk management, design control, US submissions, RA strategies for medical device development, audit/inspection support, and regulatory compliance. Medical device experience includes combination device/drug products, PPE, infusion pumps, biopsy needles & implantable markers, vertebroplasty instruments, kyphoplasty balloons, bone cement, implantable catheters, sutures, and ascites shunts.
Disclosure information not submitted.
Sponsored Presentation: Optimizing CER and PMS Document Writing with Technology and AI
Thursday, October 5, 2023
11:15 AM – 11:40 PM EDT