NAMSA
Contract Research Organization for Medical Devices and IVDs
Home
/ test course
test course
do not purchase this test course
Description
Description
nope
Search for:
Pages
Home
Sign Up Thank You
Sign Up
Account
Cart
Checkout
European Union’s General Data Protection Regulation Frequently Asked Questions – Vendors
COVID-19 Updates
European Union’s General Data Protection Regulation Frequently Asked Questions – Clients
Services
MRO Program
Product Development Strategy
Medical Writing Solutions
Medical Device Reimbursement
Biological Safety
Clinical Research
Medical Device Regulatory & Quality
IVD
Medical Device Testing
Therapeutic Expertise
Other Therapeutic Areas
Anesthesia / Respiratory
Cardiology
Dental
Dermal & Wound Care
Diabetics
Diagnostic Imaging
Ear / Nose / Throat
Gastroenterology
General & Plastic Surgery
IVD & Companion Diagnostics
Neurology
Oncology
OBSTETRICS & GYNECOLOGY (OB/GYN)
Ophthalmology
Orthopedics
Peripheral Vascular
Regenerative Medicine
Resources
Checklists and Sample Submission Forms
COVID-19 Resources
Medical Device Development Podcasts
Navigating the MedTech Start-Up World Podcast
Navigating the MedTech Start-Up World Introduction
Building your Team to Power a Successful Start-Up
Remaining Lean as a Start-Up to Brace for Longer Exits
BiocompCHATibility Podcast
Biocompchatibility – Welcome
CSI: Cracking the Case
Extractions: The How and Why
Welcome to NAMSA: Lisa Olson
NAMSA Training Series: Live from Philadelphia
NAMSA Training Series: Live from Frankfurt
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
Blog
EU MDR & IVDR Planning Resources
Resource Library
NAMSA Medical Device Test Navigators
Medical Device Test Navigator
Biocompatibility Strategy Navigator
FAQ
E-Learning
Events
Locations & Contact Information
About
Accreditations & Certifications
Our Values
Our History
Client Testimonials
Careers
Certifications and Accreditations
Site Map
NAMSA Purchasing Terms and Conditions
NAMSA’s Client Standard Terms and Conditions
Terms of Use
Privacy Policy Statement
EU-U.S. & Swiss-U.S Privacy Shield
Archives
April 2021
March 2021
February 2021
January 2021
November 2020
October 2020
September 2020
August 2020
July 2020
June 2020
April 2020
March 2020
February 2020
January 2020
December 2019
November 2019
October 2019
August 2019
July 2019
June 2019
May 2019
March 2019
February 2019
January 2019
November 2018
October 2018
September 2018
August 2018
July 2018
June 2018
May 2018
April 2018
February 2018
January 2018
November 2017
October 2017
September 2017
August 2017
July 2017
June 2017
May 2017
April 2017
March 2017
February 2017
November 2016
April 2016
Categories
Asian Market
(13)
Clinical
(9)
Clinical & Consulting
(4)
European Market
(31)
FDA
(19)
Industry Reposts
(1)
IVD
(11)
Medical Device Testing
(8)
NAMSA Press Release
(17)
Preclinical
(1)
Quality
(6)
Regulatory
(62)
Reimbursement
(2)
Toxicology
(1)
Uncategorized
(6)
