We Don't Make MedTech —
We Make MedTech Happen

Adding Expertise From Concept to Post-Market

We Don't Make MedTech —We Make MedTech Happen

MedTech is evolving — and so are we. RQM+ has long been your go-to partner for regulatory, quality, and compliance. That hasn’t changed. What’s changed is how much more we can do to support you today. As The MedTech CRO, we offer integrated clinical, regulatory, quality, and lab services — helping you accelerate development, reduce risk, and achieve global success. From startups to global manufacturers, we’re built to scale with your needs and simplify the most complex challenges.

Legacy expertise. Expanded capabilities. Continued commitment to your success.

Explore how RQM+ is redefining what a MedTech Contract Research Organization can do.

Let’s Make Your MedTech Happen

Access Device-Specific Expertise

Whatever your MedTech area of need, we’ve got you covered. Discover our expertise for your product type:  

Why RQM+?

As The MedTech CRO we deliver comprehensive, MedTech-specific solutions that help you bring life-changing innovations to market faster. Here’s how: 

We offer comprehensive services across the entire MedTech product lifecycle, from regulatory strategy and quality assurance to clinical trials, materials testing, and reimbursement — even post-market clinical follow-ups (PMCF). MedTech is all we do.

Our team consists of former FDA, MHRA, and notified body leaders; they understand regulatory processes from the inside. This expertise helps us anticipate your challenges, reduce your delays, and accelerate your approvals.

We bring deep expertise across medical devices, IVDs, SaMD/DiGA, and combination products to bear on your project. Our services cover everything from pre-clinical development to post-market support, so no matter where you are in the process, we’ve got you. 

Leveraging technology and human expertise enables us to solve complex MedTech challenges faster and with more strategic, insight-driven solutions. By combining advanced tools with deep expertise, we streamline regulatory processes and other critical functions, accelerating safer and more efficient innovation.

Whether you’re a budding startup or a global leader, we tailor our solutions to meet your needs in every project. We even offer specialized support to growing companies to help overcome resource challenges and bring products to market. 

Our strategies don’t just focus on compliance — we help you achieve regulatory success while meeting your commercial goals. We synergize regulatory strategy, reimbursement planning, and business priorities to ensure your innovations reach patients efficiently and effectively.

“The talent, expertise, and professionalism with RQM+ sets them above the other vendors I have worked with in the past. We have developed a great relationship and it has been a pleasure to work with RQM+. Thank you.”

Senior Manager, Quality Assurance, Innovative MedTech Company

“Very happy with our working relationship and have plenty more projects lined up and ready to start.”

Director, Clinical Affairs, Global Medical Device Manufacturer

Proven Track Record of Success

We’ve worked with 19 of the top 20 medical device companies and 7 of the top 10 IVD companies, delivering transformative solutions across the MedTech product life cycle. 

  • 1,000+ Clients Served

  • 5,000+ Completed Projects

  • 1,300+ Studies

  • Over 100 20+ Year Industry Veterans

Through industry-leading experts and integrated solutions in areas that are key to your product’s success, we make innovative products happen for MedTech companies around the world. 

Hear From Our Customers

“I am amazed at how much work and the number of decisions that have been made to date on this project! I really appreciate the effort and patience of your entire team!”

Director, Regulatory Affairs, Global Medical Device and Diagnostics Manufacturer

Ready to Make Your MedTech Happen?

Let’s bring your innovative MedTech products to the patients who need them.

Talk to an Expert