Biocompatibility: Documenting all the Risks

When it comes to biocompatibility, "we passed the test" may no longer be enough!

Regulatory expectations are evolving, and ISO 10993-1:2025 is changing the conversation around biological risk assessment.

So, are you documenting ALL the risks...or just the obvious ones?
Join MDG Boston for a timely discussion with two experts who know the standards inside and out (literally!):

Paolo Pescio – former Fresenius Medical Care, and a contributor to the new ISO standard
Geoff Moodie, PhD – ZOLL Medical, with 20+ years of medical device safety expertise

From raw materials to manufacturing, packaging, and beyond, we'll explore what regulators are looking for and how to stay ahead of the curve.

📅 Wednesday, October 28
⏰ 12:00–1:30 PM ET
💻 Online – Join from anywhere!

If you're in R&D, Quality, Regulatory Affairs, or Medical Device Development, this is one conversation you don't want to miss.

Because when it comes to patient safety, checking the box is just the beginning.

Register here: https://www.eventbrite.com/e/biocompatibility-documenting-all-the-risks-online-tickets-2000051581119?aff=oddtdtcreator