Erik van Dijk

Background

About Erik van Dijk

Bringing a new medical technology to market is never simple, especially for startups and scale ups navigating regulatory, technical, and business constraints all at once. That’s where I come in. I’m driven by a deep belief that meaningful MedTech innovations deserve a clear path to patients. As a former start-up CEO my self, I now help companies make smarter decisions faster, integrating regulatory and product development strategy to move forward with confidence. At MD squared, I work alongside an experienced, multidisciplinary team to guide MedTech companies through the regulatory jungle. We don’t just tick compliance boxes; we align clinical, regulatory, and business perspectives to help clients make risk-balanced, informed decisions that support both product success and commercial viability. Whether it’s defining intended use, mapping out regulatory and clinical strategy, managing risk, or designing fit-for-purpose Quality Management Systems, we help clients reduce uncertainty, avoid delays, and bring innovations to market faster. If you’re facing regulatory or business challenges in MedTech, let’s talk. I’d love to explore how we can help you cut a pragmatic path to market, without losing sight of your bigger mission.