How do you assess the extractables and leachables of a substance-based Medical device?
DeviceMed, May 2024
Interviewee
Léa Varignier, Toxicologist, Eurofins Medical Device Services France
The Transition to MDR and Important Considerations – An Orthopedic Innovators Q&A
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Lab Tested, Industry Approved: A Discussion of Ortho Device Testing & Analysis
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Addressing the Presence of Residuals in Manufacturing - A Medtech Makers Q&A
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Women in Medtech 2023: Liz Sydnor, Eurofins Medical Device Testing Director of Microbiology
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Deterministic Container Closure Integrity Testing - Navigating the Essential Techniques
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Inside Story: An Interview with Elizabeth Sydnor
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A Combined Effort for Drug Delivery & Combo Product Technology
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Inside Story: An Interview with Sunny Modi
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Combination Products: A Difficult Balance Between Drug and Device
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Inside Story: An Interview with Leonard Harris
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Inside Story: An Interview with Elizabeth Sydnor
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An Evaluation of Laboratory Testing for Orthopedic Device Makers - An Orthopedic Innovators Q&A
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Women in Medtech 2022: Susan Shorter, Eurofins Medical Device Testing, Quality, Scientific Group Leader III
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Burden of Proof: An Orthopedic Testing & Analysis Roundtable
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The Rapid Evolution of Laboratory Testing for Medical Devices - A Medtech Makers Q&A
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Inside Story: An Interview with Elizabeth Sydnor
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Packaging, Sterilization Considerations Go Part and Parcel with Product Development
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Inside Story: An Interview with Geoffrey Moodie
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New requirements for medical device cleaning validations – An overview of ST98
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Women in Medtech 2021: Liz Sydnor, Eurofins Medical Device Testing Director of Microbiology
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Eurofins Medical Device Testing helps ensure Sterile Barrier System integrity for patient safety
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Regulators enforce ISO 18562
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People are the Chemistry - Michelle Kolodziejski
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Medical Device Package Testing: Developing a Test Plan that Avoids Product Launch Delays
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Testing in Flux: Changing Protocols for a Transformative Industry
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Making the Grade: A Testing and Analysis Roundtable
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Transformative Testing: Addressing Patient Safety and Cybersecurity
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ISO 18562 Standards reduce hazards for Medical Device Breathing Pathways
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Ensuring Reusable Devices are Safe for the Next Patient
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Don’t get lost in EU Medical Device regulation harmonisationAuthor
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How to Sample and to Analyse VOCs of Respiratory Medical Devices According to the New ISO 18562-3
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Quality Assurance in the Medical Device Production Environment - Environmental Control and Identification of Microorganisms
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Testing in a Rapidly Changing World
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Developing a package testing plan that avoids product launch delays
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People are the chemistry: Andrew Blakinger
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Biocompatibility Evaluation of Breathing Medical Devices: Understanding ISO 18652
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New scenarios for biological evaluation of medical devices with new ISO 10993-1 standard
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Eurofins Medical Device Testing Launches New Package Testing Lab, Enhances Global Testing Capabilities to Support the Medical Device Industry
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A QUICK Guide to Selecting A CMO
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Packaging Validations-Looking Beyond ISO 11607
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Inside Story: An Interview with Christopher Scott
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Choose from several Container Closure Integrity Testing options
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Stuck on Instron
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People are the Chemistry - Jennifer Roark
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Considerations for Globalizing Combination Products
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The advantages of a comprehensive chemical characterization
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