Medical Device Testing
WE KNOW HOW™
Typical Medical Device Testing
EAG has over 40 years experience in medical device testing. From a single analytical support partner, clients gain expertise in chemical characterization, surface analysis, and materials chemistry.
EAG offers scientific excellence with a large number of Ph.D.s on staff. Our clients have direct access to our expertise in project design and technique selection. Through a consultative approach, these projects utilize the most appropriate techniques and clients get the right answers the first time.
We help clients maintain strict adherence to the latest regulations from Notified Bodies including the FDA and those designated under the EU MDR.
EAG reduces risk for device companies needing compliance support or facing safety challenges. All medical device testing is performed at ISO 17025 certified laboratories. By utilizing EAG’s expertise in the composition of a device, clients confidently assess their product’s safety and performance. For clients managing different supply chains, EAG reduces risk by providing redundancy of equipment and analytical services from multiple global locations.
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