Download our comprehensive NIH SBIR/STTR biotech grants toolkit covering Phase I ($285,000) and Phase II ($2,000,000) application strategies, technical proposal templates for therapeutics, medical devices, diagnostics, and digital health, clinical validation frameworks, FDA regulatory pathway planning, NIH institute-specific strategies, eligibility requirements, submission timelines, and success strategies for life sciences startups pursuing non-dilutive federal biomedical innovation funding across all 27 NIH institutes including NCI, NHLBI, NIAID, NINDS, and NIDDK supporting breakthrough healthcare solutions improving patient outcomes.
Complete scientific proposal template, clinical significance section, commercialization plan, budget justification for $285K Phase I and $2M Phase II
Detailed analysis of 27 NIH institutes with winning proposal strategies for NCI, NHLBI, NIAID, NINDS, NIDDK and disease-specific priorities
Step-by-step framework for articulating unmet medical need, patient population, clinical impact with health economics and outcomes data
Complete guide to 510k, PMA, IND, IDE pathways with clinical trial design, endpoints, regulatory milestones and approval timelines
Templates for obtaining letters of support from physician key opinion leaders at academic medical centers demonstrating clinical validation
Framework for presenting in vitro, in vivo, clinical pilot data proving proof of concept, efficacy, safety with statistical analysis
Specialized strategies for therapeutics, medical devices, diagnostics, digital health with sector examples and success stories
Line-by-line budget templates for Phase I $285K and Phase II $2M with allowable costs for biomedical R&D, clinical studies, regulatory
From cancer to cardiovascular with strategies for all 27 NIH institutes and disease priorities
Understand 510k, PMA, IND pathways with clinical trial design and regulatory milestone planning
Learn how to engage KOLs and academic medical centers for market validation and clinical studies
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