Medical Device Testing
Expert partner for mechanical testing, providing comprehensive & proven solutions. We specialize in medical device testing services.
COMPREHENSIVE PROVEN SOLUTION
Our combined services & expertise create efficiency & cohesive project knowledge from start to finish. We provide accurate quoting and guidance to complete the necessary services for your project.
WHY EMPIRICAL EUROPE
FOR MECHANICAL DEVICE TESTING?
The Empirical Method for Success is the proven process that our global clients rely on for their projects. From accurate quoting to our expert
gap analysis, our combined services will help your project to a faster path of completion. Empirical has all of the pieces for success.
- Testing
- Regulatory Approval
- Shorter Time to Market
- Faster ROI
Our Services
With over 20 years in the medical device
testing service industry, our team of experts work with top global companies who expect exceptional service and results.
Mechanical Testing service for medical devices
We offer a complete mechanical testing service package, including an unsurpassed technical report and a comprehensive partnership to guide you to successful project completion faster than our competitors.
Regulatory & Consulting
We have proven successes throughout as an FDA quality and regulatory consultant at helping our clients navigate through the process to reach their goals effectively and efficiently.
European Medical Device Regulation
From building a clear timeline to carrying out a strategic gap analysis to delivering EU MDR training for continual improvement, we assure your implementation process will reach the deadline with the specialties essential to accurately advise the transition.
FDA 510(K) Consulting
We aim to remove the stress and burden of 510(k) submission from your shoulders by bringing skill and dedication as FDA 510K consultants to the partnership, so you can enjoy a more seamless experience with desirable outcomes at the end of the submission process.
FDA Compliance Consultants
Our FDA compliance services include regulatory support, quality system development and improvement, 510(k) submission, and much more, so you can enjoy a streamlined and expedited path toward getting and keeping clearance.