Now Accepting Applications for FDA and CTTI Patient Engagement Collaborative (PEC)
Topics Included: Patient Engagement
SHARE TO:
The FDA and CTTI are currently accepting applications from patient advocates interested in becoming members of the Patient Engagement Collaborative (PEC). The PEC is an ongoing, shared forum in which the patient community (PEC members), FDA, and CTTI discuss a range of topics for enhancing communication, education, and patient engagement related to medical product regulation.
Applicants will be selected based on their ability to meaningfully contribute to the PEC, represent and express the patient voice for their constituency, work in a constructive manner with relevant individuals and organizations, and understand and navigate the clinical research system. The two-year term will begin January 1, 2025.
Successful applicants will include:
- Patients who have personal disease experience
- Caregivers who directly support patients (e.g., a family member or friend) and have personal disease experience through this caregiver role
- Representatives from patient groups who, through their role in the patient group, have direct or indirect disease experience
PEC members participate in 5-6 virtual meetings per year. Other meetings may be organized, as needed.
The following PDF format documents are required to apply and must be submitted at the same time:
- A current and complete one- to two-page resume or bio that summarizes your patient advocacy experience and related activities; and
- A one-page professional letter of endorsement from a patient group with which you have worked closely on activities that are relevant to the PEC
A maximum of 75 applicants will be considered for PEC membership and up to eight members will be selected. Interested applicants are encouraged to complete and submit the online form starting on July 9, 2024 at 11:59 p.m. A maximum of 75 completed applications will be considered.
Applications will be accepted until 11:59 p.m. Eastern Time on August 8, 2024 or until 75 complete applications are received, whichever happens first.
Those who are unable to apply electronically are encouraged to call FDA Patient Affairs at 301-796-8460 to arrange for a mail submission.
Please review the related Federal Register Notice for important information about the application process.
For more information:
Recent News Feed
- FDA, CTTI Convening 2025 Hybrid Public Workshop on Artificial Intelligence in Drug & Biological Product Development August 25, 2025

- CTTI Releases New Recommendations to Guide Use of Disease Progression Modeling in Medical Product Development July 8, 2025

- Optimizing Flexibility and Data Quality in Clinical Trials: Bringing Clarity to DIA Global 2025 June 25, 2025
