In the test, the chemicals leaching off of the device are compared with a searchable database that provides background on toxicity and the Cramer classification. The proposed change in the standard ...

Dublin, June 30, 2025 (GLOBE NEWSWIRE) -- The "Biological Evaluation of Medical Devices Training Course" training has been added to ResearchAndMarkets.com's offering. Ensure compliance with the ISO ...

Several noteworthy changes are anticipated in a new FDA guidance document on biological evaluation and biocompatibility testing of medical devices due out sometime this year. Audrey Turley There has ...

Over the last 15 years, ISO 10993-18 has become a notable resource for professionals at each stage in the supply chain and manufacturing of medical devices, assisting them in the evaluation of ...

The U.S. Food and Drug Administration (FDA) published an updated final guidance on the use of International Standard ISO 10993-1, “Biological evaluation of medical devices - Part 1: Evaluation and ...

With biocompatibility and cytotoxicity certifications, Master Bond EP21AOLV-2Med is often selected for bonding, sealing, coating and encapsulation applications in the medical device industry. This two ...

(MENAFN- GlobeNewsWire - Nasdaq) Join our seminar to master ISO 10993 compliance for medical devices, crucial for EU MDR. Learn risk management, FDA approach, and global requirements from experts.

The "Biological Evaluation of Medical Devices Training Course" training has been added to ResearchAndMarkets.com's offering. Ensure compliance with the ISO 10993 series of standards for the biological ...