Bioburden Testing vs. Sterility Testing: What Is The Difference?
Published: August 6, 2024
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Understanding the New MDCG 2024-4 Guideline for IVD Safety Reporting
Published: May 21, 2024
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Microbial Identifications: Managing Bioburden Monitoring Results
Published: May 14, 2024
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Understanding ‘Assumed Release’ in ISO 10993-17:2023
Published: April 5, 2024
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Will Vaporized Hydrogen Peroxide (VHP) Sterilization for Medical Devices Become More Common?
Published: March 20, 2024
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ASCA Accreditation: FDA Annual Report and NAMSA Customer Experience
Published: February 29, 2024
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MDR Vigilance: New MDCG Guidance Published
Published: February 13, 2024
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European Commission Updates Chemical Classification and Labeling
Published: February 2, 2024
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Pacemaker Lead Device Testing
Published: February 1, 2024
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MDCG 2022-11 Rev 1: Urgency for MDR and IVDR Compliance
Published: December 4, 2023
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Five Reasons Not to Delay Your MDR Certification
Published: December 1, 2023
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WOUNDS UK: Models and Methods to Support the Development of Novel Burn Wound Antimicrobial Treatments
Published: November 16, 2023
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FDA Announces Release of “Playbook for Threat Modeling Medical Devices”
Published: December 3, 2021
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FDA Qualifies New Cybersecurity Medical Device Development Tool
Published: April 28, 2021
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EMA Issues Q&A Regarding Impact of MDR, Article 117
Published: March 6, 2019
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Effective Implementation of EN ISO 14971 Medical Device Risk Management Standard
Published: August 15, 2018
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