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Contract Research Organization for Medical Devices and IVDs
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NAMSA Training Series: Live from Philadelphia
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Editor Chat: Biocompatibility and Performance of Medical Devices
Discussion with Chemical Characterization “A-Lister” Ted Heise on the New ISO 10993-18
Answering Your Questions on ISO 10993-18:2020
The Biological Evaluation Plan: A Manufacturer’s Perspective with Guest Dave Parente of Ecolab
Reusable Devices and the Challenges with Biocompatibility
Covid 19: Biocompatibility of Ventilators and Respiratory Devices
Listener MailBag – We Answer Your Questions
FDA and ISO 10993-18:2020
Why Biocompatibility Cares about Preclinical: NAMSA and APS Discuss
When to Go with In Vitro: Your Irritation Questions Answered
Oh No, Another Failed Cyto!
Is your Biocompatibility Program Knocking your Submission Off Track?
The Facts About In Vitro Irritation
Intact Skin Contact Devices: To Test or Not to Test
What in the World is the FDA’s Lab Accreditation Program – ASCA?
ISO 10993-4: The Second Most Misunderstood Section of 10993
Finding the Qualified Biocompatibility Unicorn
Biocompatibility and the Pre-Submission Meeting – The Devil is in the Details
A Start-up Biocompatibility Story – Prescient Surgical
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