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NAMSA eLearning ISO 10993 Series 1
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Understanding Today’s MedTech Landscape for Start-Ups: Part 1
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Talking Risk with Dr. Naveen Agarwal-Part 1
Compliance Pitfalls of In Vivo Studies—How to Learn from the Mistakes of Others
The EU IVDR: What Do You Need To Know?
Clinical Investigations: Collecting Proof That Your Device is Safe and Effective
IVD Special – Software in a Medical Device (SiMD) vs. Software as a Medical Device (SaMD): Understanding Regulatory Differences and Expectations
Software in a Medical Device (SIMD) vs. Software as a Medical Device (SaMD): Understanding Regulatory Differences and Expectations
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NAMSA Awarded ASCA Accreditation
Welcome to the RA QA Café
What Exactly is my Test Article?
Biocompchatibility – Welcome
CSI: Cracking the Case
Extractions: The How and Why
FDA Thoughts On Chemical Characterization
Don’t Forget Packaging!
Welcome to NAMSA: Lisa Olson
Editor Chat: Biocompatibility and Performance of Medical Devices
NAMSA Training Series: Live from Philadelphia
NAMSA Training Series: Live from Frankfurt
Discussion with Chemical Characterization “A-Lister” Ted Heise on the New ISO 10993-18
Reusable Devices and the Challenges with Biocompatibility
Answering Your Questions on ISO 10993-18:2020
The QB1 of GLP
Biological Equivalency: When is “same” the same?
The Biological Evaluation Plan: A Manufacturer’s Perspective with Guest Dave Parente of Ecolab
Biocomp and Beer
Covid 19: Biocompatibility of Ventilators and Respiratory Devices
Biocompatibility FAQ
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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