OTTAWA, ON, April 29, 2025 /CNW/ - Spiderwort Biotechnologies Inc., a pioneering biotechnology company focused on cellulose-based regenerative medicine, today announced the completion of ISO 10993 ...

Dublin, June 23, 2022 (GLOBE NEWSWIRE) -- The "Biocompatibility Testing: What You Need to Know" training has been added to ResearchAndMarkets.com's offering. The objective of the Seminar is to teach ...

Brinkman brings more than 15 years of experience in biological sciences and is known for her rigorous, clinically relevant approach to biological risk evaluation "We're thrilled to welcome Katie to ...

In April 2013, FDA released draft guidance for industry and FDA administration staff titled “Use of International Standard ISO 10993, ‘Biological Evaluation of Medical Devices Part 1: Evaluation and ...

Image of an in vitro irritation test courtesy Nelson Laboratories. Biocompatibility testing requirements for medical devices are changing. "A lot of things are happening, on all fronts," Thor Rollins, ...

(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.

Dublin, June 13, 2019 (GLOBE NEWSWIRE) -- The "Biocompatibility Testing for Medical Devices" conference has been added to ResearchAndMarkets.com's offering. The medical device field is one of the most ...

Cellulose dermal filler achieves critical biocompatibility milestones, paving the way for clinical trials OTTAWA, ON, April 29, 2025 /CNW/ - Spiderwort Biotechnologies Inc., a pioneering biotechnology ...