Канал: Eurofins Medical Device Testing

Maintain Sterile Barrier Integrity with Eurofins

Maintain Sterile Barrier Integrity with Eurofins

Extractables & Leachables Testing via new technology. Agilent 6546 Q-TOF LC-MS Preview

Extractables & Leachables Testing via new technology. Agilent 6546 Q-TOF LC-MS Preview

Endure Storage with Eurofins’ Shelf Life Testing

Endure Storage with Eurofins’ Shelf Life Testing

Ensure Your Device Survives Global Transport

Ensure Your Device Survives Global Transport

Your Trusted Package Testing Partner

Your Trusted Package Testing Partner

Packaging Validation of Medical Devices - Impact of the Revisions of ISO 11607 & Suitable Strategies

Packaging Validation of Medical Devices - Impact of the Revisions of ISO 11607 & Suitable Strategies

Testing Requirements for a Successful Sterilization Validation

Testing Requirements for a Successful Sterilization Validation

Chemical Characterization/Toxicological Risk Assessments: A Smart Approach to Biological Evaluation

Chemical Characterization/Toxicological Risk Assessments: A Smart Approach to Biological Evaluation

Chemical Characterization: How to Initiate the Biological Evaluation of Medical Devices

Chemical Characterization: How to Initiate the Biological Evaluation of Medical Devices

Threat Modeling Medical Devices

Threat Modeling Medical Devices

Container-Closure Integrity Testing for Drug Delivery Devices

Container-Closure Integrity Testing for Drug Delivery Devices

Package Testing: Developing a Test Plan that Avoids Product Launch

Package Testing: Developing a Test Plan that Avoids Product Launch

Sterility Validation 101: Ensuring a robust sterilization validation program from start to finish

Sterility Validation 101: Ensuring a robust sterilization validation program from start to finish

Biological Evaluation of Breathing Gas Pathways of Medical Devices, A New ISO Standard

Biological Evaluation of Breathing Gas Pathways of Medical Devices, A New ISO Standard

Endotoxin Testing: Make Sure FDAs New Guidance Doesn’t Delay Your Product Launch

Endotoxin Testing: Make Sure FDAs New Guidance Doesn’t Delay Your Product Launch

Biocompatibility Testing of Combination Products & Medical Devices: New Regulatory Guidance

Biocompatibility Testing of Combination Products & Medical Devices: New Regulatory Guidance

Developing a Testing Plan for Medical Device Design Verification

Developing a Testing Plan for Medical Device Design Verification

Biocompatibility Basics: Making sense of the Annex A Matrix

Biocompatibility Basics: Making sense of the Annex A Matrix

Chemical Characterization: The Starting Point for Biological Evaluations

Chemical Characterization: The Starting Point for Biological Evaluations

Developing Test Strategies Per the New ISO 10993-1: Current Status and Upcoming Changes

Developing Test Strategies Per the New ISO 10993-1: Current Status and Upcoming Changes

Changes in Europe’s Medical Device Regulations: Consequences for Manufacturers

Changes in Europe’s Medical Device Regulations: Consequences for Manufacturers