Senior RA Manager
Elva brings over 15 years of medical device industry knowledge across regulatory affairs and quality. In her current role, Elva leads a team of regulatory professionals who provide regulatory strategy, submission authoring and product life cycle management, to enable business development initiatives in the global markets in US, EU, China, APAC, Latin America and worldwide.
Elva is RAPS RAC (US, EU, CAN, GS) and ASQ CQA certified and specializes in the medical device products industry for global market regulatory compliance. She has served in several regulatory affairs and quality management roles with Medtronic, Hillrom, Siemens and GE Healthcare, etc.
Monday, September 14, 2020
10:00 AM – 11:30 AM EDT