This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Regulation, Clinical and Software for Medical Devices
November 5 - 7, 2024
Digital Conference8:00AM CST // 9:00AM EST // 2:00PM GMT

Camie Meller
Associate Director of Medical Affairs at BD Urology and Critical Care
Speaker

Profile

Camie is an Associate Director of Medical Affairs at BD Urology and Critical Care where she leads the Clinical Sciences Team responsible for evaluation, documentation, and generation of clinical evidence. Camie has been the EU MDR Medical Affairs Lead at UCC for the past 5 years, managing the clinical requirements for successful remediation from MDD to MDR for a diverse portfolio of products across all device classifications.

Camie has experience in developing clinical evidence strategies to support new product development as well as strengthening in-market products with post-market clinical follow up data. She has over 10 years of Medical Affair experience at BD (and previously C.R. Bard) with over 20 years in total of biotech and academic research and product development.

She is a Board Certified Medical Affairs Specialist and completed a certificate in Design and Interpretation of Clinical Trials through Johns Hopkins University. Camie holds a bachelor’s degree in Microbiology and a master’s degree in Animal Sciences from Oregon State University. She also earned a doctorate in Biology from Portland State University.

Agenda Sessions

  • Industry Perspective: Navigating the Clinical Evaluation Documentation Web

    11:55am