At AR2-C2, we’re redefining the game by merging AR support with clinical and marketing strategy.
While many startups worry about Europe’s stringent MDR and IVDR regulations, we see an opportunity. Startups need to improve their devices‘ worth to investors, and nothing beats real-world success in a competitive market, especially when certified by the toughest notified bodies.
That’s where we come in. We’re not your average authorized representative service provider. We’re the link between regulatory market access, clinical data, and your marketing strategy. We’re AR2-C2.
In Europe, if you can make it here, you can make it anywhere!“
Join us on September 26th in Munich for an intensive hands-on bootcamp designed to equip you with the tools you need to master regulatory and reimbursement strategies for your HealthTech and MedTech innovations. With limited spots available, register now to secure your place and take the next step toward market success!
On August 24th, we embarked on a remarkable journey! With over 100 years of collective expertise in medical devices, in vitro regulations, clinical strategy, business development, and European healthcare reimbursement, we’re here to make a difference.
Our mission is clear: to empower medtech companies at every stage of their journey. From crafting robust clinical and regulatory strategies to nurturing business development, navigating European healthcare reimbursement, guiding you through CE certification, liaising with Notified Bodies, managing audits, and acting as your trusted Authorized Representative – we’ve got you covered.
Join us on this incredible journey as we help shape the future of healthcare innovation. Together, we’ll turn challenges into opportunities and pave the way for groundbreaking solutions. Stay tuned for exciting updates and insights!