The CRO Group > Services

Regulatory & Compliance Consulting Expertise

The CRO Group offers a wide range of development, QA, regulatory, and clinical consulting services to medical device and IVD companies around the world.

HOW YOU KNOW IF YOU NEED REGULATORY & COMPLIANCE CONSULTING:

Ever feel overwhelmed by the FDA, Notified Body or Competent Authority, or other Regulatory Agency? Or that the maze of regulations needing to be navigated had no way out? Maybe that next milestone is very critical to your funding and getting there seems a bit challenging? Perhaps you have too many consultants or too few or the ones you have just provide cookie cutter results?

Each of these scenarios is exactly why clients call us. Our response is to meet those milestones cost-effectively and get you to the next step in your development process. Our expert regulatory affairs and compliance consultants do this by telling you exactly what you need to know—not necessarily what you want to hear—but the reality of the situation you face. We let you know what the real budget is and how long it will really take to get where you want to go.

WHY CHOOSE THE CRO GROUP?

For over 30 years, The CRO Group has made sure clients achieve their device development and premarket goals. Since 1996, we have spent more time figuring out what our clients need than many firms have been in business. Along the way, we have helped achieve the processes required to get their medical devices and mobile applications to the next step.