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What we do

From early development to market launch—we help you get it right.

Biotech and pharma leaders come to us when they need a clear, integrated strategy that aligns clinical development, regulatory pathways, market access, and commercial goals. We bring deep experience, structured thinking, and a focus on what actually drives product success.

Whether you're preparing for a board milestone, refining your go-to-market plan, or course-correcting mid-development—this is how we help.

Our
Signature Methodology

We follow a structured three-step approach that adapts to your situation—but always delivers clarity and actionable direction.

Step 1: Strategic Assessment

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We start with a sharp analysis of your current plans, data, assumptions, and stakeholder alignment. This includes:
 

  • Development strategy and clinical rationale

  • Regulatory milestones and risks

  • Market access implications

  • Competitive positioning
     

You’ll know what’s working, what’s missing, and what needs to change.

Dr Georg van Husen leads the way

Step 2: Scenario Design

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We develop and pressure-test strategic options—tailored to your compound, portfolio, or market goals.
 

  • What trade-offs are you facing?

  • What would a smarter pathway look like?

  • How can you future-proof key decisions?
     

You’ll see the full picture—risks, benefits, timelines, and evidence needs.

Dr Georg van Husen leads the way

Step 3: Integrated Strategy

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We help you consolidate the best path forward—linking development, regulatory, and commercial thinking into a cohesive, investor-ready strategy.
 

You walk away with alignment, confidence, and a plan you can execute.

Dr Georg van Husen leads the way
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