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🧬 Free Life Sciences Download

Canada Life Sciences Grants Application Toolkit

Get instant access to comprehensive biotechnology funding guide with IRAP biotech templates, clinical trials checklists, medical device regulatory tools, and biomanufacturing frameworks used by life sciences companies to secure $95M+ across 18+ drug development and health technology programs.

What's Included in Your Life Sciences Toolkit

IRAP Biotech Application Templates
  • Complete IRAP life sciences project template (up to $500K)
  • Drug development technical feasibility framework
  • Biotech IP protection and FTO analysis templates
  • Therapeutic target validation documentation
Clinical Trials Application Kit
  • CIHR clinical trials grant application template
  • Clinical trial protocol (CTP) framework
  • Patient recruitment and retention strategies
  • Health Canada CTA submission checklist
Medical Device Regulatory Tools
  • Health Canada MDEL submission templates
  • Medical device classification guide (Class I-IV)
  • FDA 510(k) regulatory pathway comparison
  • ISO 13485 QMS implementation checklist
Biomanufacturing & Scale-Up Tools
  • GMP facility funding application templates
  • Biomanufacturing cost analysis calculator
  • Cell and gene therapy manufacturing guidelines
  • Multi-program funding stacking strategies

Bonus: Expert Life Sciences Consultation

Download includes a complimentary 30-minute life sciences funding strategy consultation with our biotech specialists who have secured $95M+ in drug development and medical device grants with 76% success rate.

Download Your Free Life Sciences Toolkit

Join 2,200+ biotech innovators who've accessed our life sciences funding resources

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Trusted by Life Sciences Leaders

$95M+
Biotech Grants Secured
76%
Success Rate
2,200+
Downloads

What Life Sciences Innovators Say

"The IRAP biotech templates and clinical trial checklist helped us secure $420K for our rare disease drug development. The regulatory guidance was spot-on."

Dr. Rachel Chen
CSO, GeneTheraPharma

"The medical device regulatory tools and MDEL templates saved us months. We navigated Health Canada approval smoothly for our Class III device."

Michael Rodriguez
CEO, MedDevice Solutions
FSI Digital

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Last updated: January 2025

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