Medical device controls must withstand disinfection, seal out fluids, and be usable with gloves. Failures appear as cleaning ...
By Joseph M. Saunders, Founder and CEO, RunSafe Security A medical device cleared today may stay in clinical service for 15 ...
The new ISO Class 8 clean room in Tecate, Mexico, marks the latest expansion in Arterex's aggressive 2026 growth strategy ...
For medical device assembly, maximum precision in the application of adhesives, coatings, or potting compounds is vital.
Wearable diagnostics, implantable monitors, and minimally invasive surgical instruments fuel demand for smaller components.
HiArc to showcase integrated control system HiArc Ctrl at ADLM 2026 ADLM 2026, July 26–30, Anaheim Convention Center, Anaheim ...
Nine requirements management tools for medical device development ranked by traceability, compliance support, and regulatory readiness for FDA and EU MDR.
Many modern technologies, from optical communications and artificial intelligence (AI) hardware to advanced sensors and ...
ESCATEC has achieved ISO 13485:2016 certification at its UK manufacturing facility, expanding the electronics manufacturing ...
Regulatory expert Jessica Schafersman explains why device startups must integrate FDA compliance from concept phase, not ...
In the first part of an AI-powered investigation, we reveal the death and injury toll of Australia’s medical device industry.
At the ADLM Clinical Lab Expo 2026, G&H will showcase how diagnostic and medical device companies can accelerate the ...
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