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Fractional Leadership and Management Consulting for the Life Sciences
Go-To-Market • Market Intelligence • Capital Advisory • Regulatory Affairs
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Our Services
Based in San Diego, CA, we provide management consulting and fractional leadership for the life sciences aligning strategy, systems, process, and execution to turn innovation into sustainable growth.
Go-to-Market Strategy & Launch Excellence
Comprehensive launch strategy that creates immediate market impact.
- New product introduction (NPI) process development and ideal customer profiling
- Value proposition creation, messaging frameworks, and competitive positioning
- Pricing strategy development and distribution channel identification
- Sales strategy design and go-to-market launch plan creation
- Campaign playbook development with defined metrics and KPIs
- End-to-end launch execution support from planning through market entry
Market Intelligence
Providing actionable information to life science companies.
- Industry characterization and competitive landscape analysis to map the market terrain
- Voice of customer studies and unmet needs analysis through primary market research
- Top-down and bottom-up market modeling to quantify opportunity size and addressable segments
- Revenue modeling using adoption curves built from survey data and historical proxies
- Literature review and technical analyses to inform product positioning
- Strategic insights synthesis, translating data into actionable recommendations
Capital Advisory
Strategic consulting on investor relations for life sciences and diagnostics companies.
- Investor targeting, outreach programs, and non-deal roadshow facilitation
- Quarterly earnings call script preparation and financial communications strategy
- Compelling investor presentations, corporate decks, and fact sheet development
- Financial modeling, valuation analysis, and competitive market positioning
- Crisis communication and shareholder trust management
- C-suite training on investor communication best practices and media relations
Regulatory Affairs &
Quality Assurance
Regulatory and quality pathways for companies preparing for commercialization.
- Scalable QMS design and implementation aligned with ISO 13485, FDA QSR, and global standards
- FDA, Health Canada, EU MDR/IVDR, and TGA filing preparation to accelerate market access
- Regulatory strategy for AI-powered and software-based medical devices (SaMD)
- Gap assessments, audit readiness, and supplier qualification programs
- Post-market surveillance and vigilance to maintain product compliance
- Leadership coaching on regulatory readiness, inspection prep, and quality culture
Let's Build What's Next. Together.
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