Life sciences
Grant writers who speak your science

Why life sciences applications fail
Strong science, weak proposal. The most common reasons we see: aims that aren't hypothesis-driven, no clear go/no-go milestones, missing power calculations, a regulatory pathway that reviewers can't follow, and a commercialization plan written as an afterthought.
We fix all five, in your own scientific voice, backed by writers who have sat on the research side of the bench.
Where we work
Therapeutics & drug discovery
Small molecule, biologics and cell & gene programs. Target validation through IND-enabling studies.
Diagnostics & devices
Assay development, point-of-care platforms, imaging and Class II/III device pathways.
Digital health & AI
Clinical decision support, remote monitoring and AI/ML models with a credible validation plan.
Research tools & bioprocessing
Instruments, reagents, organoids, lab automation and manufacturing scale-up.
Building a therapeutic, diagnostic or medical device? Read our NIH SBIR guide for biotech and life sciences founders.
Programs we target
NIH SBIR/STTR
Institute-specific topics with hard-science review panels. Phase I typically up to ~$300K, Phase II up to ~$2M.
NSF SBIR
Biotechnology is one of NSF's funded areas. Ideal for platform technologies that cut across health and industry.
ARPA-H, BARDA & DoD
Mission-driven health programs for high-risk, high-reward and defense-relevant medical innovation.
The NSF route, stage by stage
Biotechnology is one of the areas NSF funds, and many life sciences platforms score better at NSF than at NIH. Here is what each stage involves.
NSF Project Pitch
Gateway to a Phase I invitation
Read the NSF Project Pitch guideNSF SBIR Phase I
Up to $305,000
Read the NSF SBIR Phase I guideNSF SBIR Phase II
Up to $1,000,000
Read the NSF SBIR Phase II guidePhase II supplements
Additional funding on top of Phase II
Read the Phase II supplements guideNSF STTR
Same award levels as SBIR Phase I and II
Read the NSF STTR guideLet's fund your science
Book a free consultation with a grant writer who understands your therapeutic area or device pathway.