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How to Manage Massive Medical Device Packaging Changes

How to Manage Massive Medical Device Packaging Changes
Abhishek Gautam, director of global packaging for medical device manufacturer Teleflex, shares tips on how to stay ahead of risks while addressing your legacy packaging designs and testing to comply with the European Union Medical Device Regulation (EU MDR).
When a regulatory change requires you to revisit your legacy product testing or update virtually all your package designs, the massive workload could be daunting, especially for small or busy packaging departments. But the situation also gives you the unique opportunity to reimagine your packaging for cost reduction, production performance, and perhaps most importantly user experience and safety. ....

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EAG Expands Medical Device Testing Services with New Laboratory

EAG Expands Medical Device Testing Services with New Laboratory
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EAG Laboratories: EAG Expands Medical Device Testing Services with New Laboratory

EAG Laboratories: EAG Expands Medical Device Testing Services with New Laboratory
EAG Laboratories is expanding its medical device testing capabilities with a new 20,000 square-foot laboratory located in St. Louis, Mo.
The new laboratory is a bespoke design to support the requirements of the medical device industry. It increases EAG s analytical capabilities, allows for improved turnaround times and helps meet evolving requirements from the FDA as well as the European Union Medical Device Regulations (MDR).
Specialty features of the laboratory include:
A cleanroom designed for particle isolation and identification
A dedicated medical device polymer analysis laboratory
State-of the-art instrumentation to support biocompatitility testing of ISO 10993-18 programs for medical devices and combination products ....

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