rqm+_live_81_knowledge_center-min

Available on demand.
 
RQM+ welcomes Michelle Tarver, M.D., Ph.D., Acting CDRH Director and Deputy Center Director for Transformation, FDA, CDRH, to a presentation and panel discussion aimed at increasing awareness and understanding of equity in the medical device and IVD space.
 

Objectives:

  1. Regulatory Expectations
    Examining health equity concerns, regulatory efforts to promote equity, and FDA requirements for enhancing diversity in clinical trials

  2. Healthcare at Home
    Exploring the "Home as a Healthcare Hub" initiative and its implications for health equity, including the challenges and opportunities of integrating healthcare services at home

  3. Industry Perspectives
    Providing insights from industry leaders on how medical device companies are addressing health equity, with a focus on real-world examples and action plans

  4. Action Plans and Strategies
    Sharing best practices for developing and implementing plans that assess diversity, explore risks, and identify actions to address health equity within medical device companies

  5. Interactive Q&A
    Offering an opportunity for participants to engage with experts, ask questions, and gain a deeper understanding of the topic

Complete the form on this page to watch the recording and download the slides.

Panelists:
  • Michelle Tarver, M.D., Ph.D. – Acting Director and Deputy Center Director for Transformation, FDA, CDRH
  • Allison Komiyama, Ph.D., RAC – Vice President, MedTech Innovations, RQM+
  • Jon Gimbel, Ph.D. – Vice President of Technical, RQM+
  • Brandy Chittester – Senior Director, Clinical Operations, RQM+
  • Jaishankar (Jai) Kutty, Ph.D. – Vice President, Global Regulatory Affairs, RQM+ (moderator)

Certificate of Participation available upon request for live attendees.

Watch the Recording and Download Michelle's Slides 📥