
Session Overview
The Congressionally Directed Medical Research Programs (CDMRP), managed by the U.S. Department of War, funds high-impact biomedical research that addresses critical gaps in military and civilian healthcare. Unlike traditional funding mechanisms, CDMRP programs are mission-driven, topic-specific, and shaped by congressional intent and stakeholder input, including patients, clinicians, and advocacy groups.
Successfully securing CDMRP funding requires a clear understanding of program announcements, award mechanisms, and evaluation criteria. Applicants must strategically align their proposals with the intent of the specific research program, demonstrate strong scientific and clinical impact, and ensure strict compliance with submission and regulatory requirements.
In this session, Dr. Kelsey McLaughlin from Eva Garland Consulting (EGC) provides a practical overview of how to navigate CDMRP funding opportunities for success. The presentation covers how to identify appropriate program announcements, interpret intent language, select the right award mechanism, prepare competitive pre-applications and full proposals, and avoid common compliance pitfalls. Attendees gain insight into positioning their technology or therapeutic approach to meet both military relevance and broader healthcare impact.
Session Recap
- How CDMRP differs from NIH and other federal funding agencies
- The role of congressional intent and stakeholder-driven priorities
- Annual program announcements and evolving topic areas
- Differences between Idea Development, Clinical Trial, Translational Research, and Technology/Therapeutic Development Awards
- Matching project maturity to mechanism expectations
- Importance of clearly addressing the funding opportunity’s intent
- White paper/pre-application requirements and screening process
- Scientific peer review and programmatic review considerations
- Crafting a compelling impact statement and military relevance narrative
- Required registrations (SAM.gov, Grants.gov, eBRAP)
- Managing strict formatting, page limits, and submission deadlines
- Avoiding common administrative disqualifications
- Demonstrating patient impact and clinical relevance
- Building strong multidisciplinary teams and partnerships
- Planning for regulatory and commercialization pathways
Attendees leave with a clearer understanding of how to interpret CDMRP program announcements, strategically position their research, and develop competitive proposals aligned with Department of War healthcare priorities.


