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  1. Development & Approval Process (CBER)

Center for Biologics Evaluation and Research Patient Engagement Program

Bringing the Patient Voice into Medical Product Development

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Patient input is a critical part of the Center for Biologics Evaluation and Research’s (CBER) understanding of diseases and conditions. Engaging with patients and listening to their perspectives on their diseases and treatments may help the Center advance patient-focused medical product development. The development of patient input methods is included in the CBER Interim Strategic Plan FY 2017-2019 (Objective 5.3). Supported by provisions in both the 21st Century Cures Act of 2016 and the Food and Drug Administration Reauthorization Act of 2017, CBER’s patient engagement program is committed to incorporating patient involvement in the Center’s regulatory work.

Advancing Patient Engagement and Patient-Focused Drug Development at CBER

CBER supports Agency-wide efforts to advance patient engagement and patient-focused medical product development

CBER interacts with patient groups on Center-specific topics and actively engages in Agency programs, initiatives, and events to gather patient input and share best practices for involving patients in medical product development and regulation. CBER’s patient engagement program collaborates closely with the Center for Drug Evaluation and Research (CDER), the Center for Devices and Radiological Health (CDRH), the Office of the Commissioner and other FDA offices and programs to coordinate patient engagement activities and patient-focused medical product development efforts, and to share best practices.

Programs at CBER that support advancement of patient engagement and patient-focused medical product development include CBER’s Science of Patient Input (SPI) initiative and CBER’s Rare Disease program. SPI initiative activities include supporting studies on methods and tools to obtain robust patient input to support biological product regulatory reviews and providing CBER reviewers with assistance in the regulatory review of patient input and patient-reported outcomes data. CBER’s Rare Disease program works to facilitate the incorporation of the patient perspective in regulatory decision making for biologics for rare diseases.

CBER and CDRH collaborate on the following guidances about including patient input in the development, evaluation, and post-market surveillance of medical devices:

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CBER Engagement with Patient Organizations

CBER engages patient organizations on disease- and therapy-specific issues.

CBER staff make every effort, subject to staff resources and availability, to hear directly from patients about the burden of disease, the impact of treatment on patients, and other information that could inform regulatory decision making. This includes:

  • Learn About FDA Patient Engagement
    Information about how patients and stakeholders can engage with FDA centers and offices, including CBER
  • FDA-Led Patient-Focused Drug Development Meetings
    Meetings held by CBER and CDER between 2013 and 2017 to systematically obtain the patient perspective on specific diseases and their treatments
  • Externally-Led PFDD Meetings
    CBER participates in this FDA program that welcomes patient stakeholder organizations to generate public input on disease areas using FDA-led PFFD meetings as a model
  • External Resources or Information Related to Patients’ Experience
    A pilot webpage of links to certain publicly available reports and resources relating to patient experience data submitted by the public. NOTE: FDA reviews the materials at these links to ensure they are within the scope of the webpage, but FDA does not assess their scientific merit or compliance with regulatory requirements.

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Request a Patient Organization Meeting with CBER Staff

Meetings between patient organizations and CBER staff present opportunities to enhance CBER’s understanding of disease burden and the impact of treatment on patients. These meetings may also help to inform efforts by patient organizations working to advance drug development such as developing or conducting natural history studies or patient input studies to support medical product development.

To request a meeting with CBER staff, a representative from a patient organization can email CBERPatientEngagement@fda.hhs.gov. CBER will review requests and make every effort to hear directly from patient organizations according to staff availability and resources.

If a patient organization requests a meeting with topic that applies to more than one medical product type, the organization can submit a request through the FDA Request to Connect page. FDA Request to Connect can also help patient organizations that are unsure which FDA center or program to contact about engaging with FDA.

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Your organization’s activities, for example
  • Natural history studies
  • Patient-reported outcomes studies
  • Patient surveys on risks, benefits, and preferences related to treatments
Impact of the disease and its treatment
  • Chief complaints (most bothersome signs and symptoms)
  • Burden of living with and managing a disease or condition
  • Impacts from a disease or condition on activities of daily living and functioning
Perspectives about current and potential treatment approaches
  • Expectations of benefits
  • Tolerance for harms or risks
  • Patient preference
  • Unmet medical needs
Clinical trial considerations
  • E.g., views on various therapies, such as gene therapy
  • Burden of participating in clinical studies
  • Risk tolerance

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