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Join NAMSA for a first-of-its-type podcast series, “BiocompCHATibility,” as each episode features leading industry experts and discussion on how to proactively address specific medical device evaluation scenarios and challenges. Experts will also share real world examples and experiences focused on solutions proven to be successful.

 

TOPIC

RELEASE DATE
Navigating Biocompatibility in Early Feasibility Studies July 30, 2024
Exploring Equivalency in Biocompatibility July 9, 2024
Chemistry with the MFDS November 15, 2023
New FDA Biocompatibility Guidance – Let’s Discuss October 4, 2023
Welcome to the RA QA Café February 8, 2023
What Exactly is my Test Article? July 26, 2022
FDA Thoughts on Chemical Characterization March 30, 2022
Don’t Forget Packaging! February 23, 2022
Biological Equivalency: When is “Same” the Same? November 30, 2021
The QB1 of GLP September 30, 2021
Biocomp and Beer August 9, 2021
NAMSA Awarded ASCA Accreditation July 28, 2021
Biocompatibility FAQ June 2, 2021
Why Biocompatibility Cares about Preclinical: NAMSA and APS Discuss March 24, 2021
When to Go with In Vitro: Your Irritation Questions Answered February 23, 2021
Is your Biocompatibility Program Knocking your Submission Off Track? January 27, 2021
Oh No, Another Failed Cyto! December 23, 2020
Intact Skin Contact Devices: To Test or Not To Test November 25, 2020
What in the World is the FDA’s Lab Accreditation Program – ASCA? October 28, 2020
The Facts About In Vitro Irritation September 30, 2020
ISO 10993-4: The Second Most Misunderstood Section of 10993 August 26, 2020
FDA and ISO 10993-18:2020 July 22, 2020
Listener MailBag – We Answer Your Questions July 22, 2020
Finding the Qualified Biocompatibility Unicorn June 24, 2020
Biocompatibility and the Pre-Submission Meeting – The Devil is in the Details May 27, 2020
A Start-Up Biocompatibility Story – Prescient Surgical April 22, 2020
Covid 19: Biocompatibility of Ventilators and Respiratory Devices April 6, 2020
Reusable Devices and the Challenges with Biocompatibility March 25, 2020
Answering Your Questions on ISO 10993-18:2020 February 14, 2020
The Biological Evaluation Plan: A Manufacturer’s Perspective with Guest Dave Parente of Ecolab January 23, 2020
Discussion with Chemical Characterization “A-Lister” Ted Heise on the New ISO 10993-18 December 18, 2019
Editor Chat: Biocompatibility and Performance of Medical Devices December 3, 2019
NAMSA Training Series: Live from Frankfurt November 14, 2019
NAMSA Training Series: Live from Philadelphia October 29, 2019
Welcome to NAMSA: Lisa Olson October 10, 2019
Extractions: The How and Why September 12, 2019
CSI: Cracking the Case September 12, 2019
Welcome September 12, 2019

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