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FDA Releases CDRH Health of Women Strategic Plan to Better Inform Medical Device Research and Regulation for All Women

For Immediate Release:
Statement From:

Terri Cornelison, M.D., Ph.D.
Chief Medical Officer and Director, Health of Women Program – Center for Devices and Radiological Health

Today, as part of the U.S. Food and Drug Administration’s continued commitment to protect and promote the health of all women, the Center for Devices and Radiological Health (CDRH) is sharing its Health of Women Program Strategic Plan. CDRH initially issued a proposed strategic plan in September 2019 and has considered public feedback to inform this strategic plan, which lays out the framework to further the FDA’s mission by protecting and promoting the health of women, strengthening regulatory science, and identifying and addressing current and emerging issues in medical device research and regulation for the health of all women.

As scientists and the medical community continue to learn more about sex and gender differences, we are learning that both sex—an individual’s biological characteristics—and gender—the social construct by which one may define oneself —may play significant roles in the course and outcome of conditions that affect all human organ systems. While sex and gender are interrelated, they are not necessarily mutually exclusive, and their interactions may affect physiological reactions, presentation of disease and treatment outcomes.

Now more than ever, we need to understand the implications sex and gender present for the performance of medical devices in all individuals. The CDRH Health of Women program is a comprehensive, collaborative, landmark program built on the premise that both sex and gender have a considerable impact on a woman’s overall health, not just their reproductive or sexual health. With patients at the heart of this initiative, and with the strategic plan as a blueprint for the center’s priorities, Health of Women intends to ensure all women have access to innovative, safe and effective medical devices.

The CDRH Health of Women Program

The CDRH Health of Women program was created in 2016 to address the steadily growing importance of sex- and gender-specific issues arising from medical technology design and development, clinical trial design and other medical device-related matters. Since its start, the program has been working toward a better understanding of how medical devices—those developed specifically for women as well as those developed for people of all sexes and genders—perform in women and exploring unique issues in the regulation of medical devices related to the health of women.

Historically, biomedical research—from non-clinical cell research to animal studies to clinical human research—has overwhelmingly been conducted in patients assigned as male at birth. Representation in research is crucial to understand how medical products, including medical devices, interact with individuals of different sexes and genders. A lack of representation can have serious consequences for health outcomes for women. An example of this is cardiovascular devices like pacemakers that may have different outcomes and complication rates in men and women. This is just one instance of when sex and gender make a difference in designing a clinical study that will provide optimal results for safety and effectiveness for all patients.

CDRH Health of Women Strategic Plan

With the knowledge that sex and gender differences factor into a person’s unique experience with medical devices and treatment outcomes, the CDRH Health of Women Program created its strategic plan in 2019. At that time, the FDA sought input from the public and other stakeholders on the contents of the plan. Since then, CDRH has considered that feedback, along with other lessons learned, to finalize the framework. The integrative, cross-cutting plan, which prioritizes the patient experience and leverages partnerships across CDRH, aims to establish a portfolio of women-specific device efforts and strategize around gap areas to inform our research.

The strategic plan lays out the program’s three main priorities:

  • Sex- and Gender-Specific Analysis & Reporting—Improve availability, analysis and communication of sex- and gender-specific information for the safe and effective use of medical devices to improve and better understand the performance of medical devices in women; optimize CDRH practices for consistent sex- and gender-specific data collection, analysis and reporting; ensure CDRH’s policies evolve with current science.
  • Integrated Approach for Current & Emerging Issues Related to the Health of Women—Strengthen internal health science programs and initiatives across CDRH, working together with CDRH offices and our stakeholders, to create actions that aim to improve the overall health and quality of life for women; coordinate and lead an integrated approach to analyze current and emerging issues related to the health of women; explore innovative strategies, technologies and device-specific study paradigms; develop center-wide policies and outreach activities related to the health of women.
  • Research Roadmap—Develop a guide for navigating the health of women medical device ecosystem; address identified gaps and unmet needs related to the health of women through targeted resources; promote advancement of regulatory science related to the health of women.

With the implementation of these three strategic priorities, we aim to deepen our understanding of how medical devices work for women and continue our efforts to help assure that medical devices – those developed specifically for women, and those developed for all people – optimally align with the considerations of usability and performance in women. In this way, we hope to achieve the highest quality of innovation, safety and effectiveness for every patient.

Related Information

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The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.


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