Guides

Staying Ahead of Dutch DBA Regulations in 2025

With record-breaking investment, faster regulatory pathways, and stronger returns, the US has become the next strategic move for many European life sciences companies. But success in this market isn’t just about timing - it’s about understanding what’s different and planning accordingly. This guide breaks down the opportunities, challenges, and critical factors behind a successful US expansion strategy in 2025.

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Why this report matters

From FDA credibility to funding access and proximity to innovation hubs, the US market offers enormous upside, but it also brings fierce competition, high operational costs, and cultural differences that can’t be ignored.

This guide helps you weigh the pros and cons with clarity and confidence, so you can decide if (and when) US expansion is the right next step.

Whether you’re planning your first hire stateside or preparing to scale a commercial team, this is essential reading.

 

If you're exploring US expansion in 2025, this guide gives you the strategic insight to move forward with focus.

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Why This Guide Will Transform Your Hiring Process

Understand how healthcare spending, talent access, and regulatory frameworks differ between the EU and the US so you can position your strategy with a global perspective.

Explore where and how EU life sciences companies are unlocking US investment and what it means for scaling, localisation, and competitive advantage.

Gain clear insights into FDA fast-track pathways and other credibility signals that support market entry and accelerate development timelines.

Recognise the hurdles from differing cost dynamics to team alignment across regions so you can anticipate risks and mitigate them early.

Learn practical lessons on recruiting locally, winning capital, and launching successfully — based on how others have done it, not just theory.

Use comparative data and hands-on guidance to shape confident, forward-looking strategies for entering and thriving in the US market.

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