Compliance with Clarissa - 2023
Episode 31: "PFAS in Medical Devices" with Matt Quinn
19 December 2023
Episode 29: "Satellite Data Acceptance" with Tom Van Luven
09 November 2023
Episode 28: "SaMD" with Cyrus Ahmadi
31 October 2023
Episode 27: "UKCA for Medical Devices" with Sharmila Gardner
17 October 2023
Episode 26: "Cybersecurity By Design" with Wayne Stewart
03 October 2023
Episode 25: "Intertek in the Med Device Industry" with Sunny Rai
07 September 2024
Episode 23: “Product Certification” with Matt Snyder
09 August 2023
Episode 14: “The Benefits of Performance Testing” with Alex Porter
09 February 2023
Related Links
Medical Podcast - Compliance with Clarissa
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Knowledge Center
Download the latest information from our medical device compliance experts.
Machine Learning and Artificial Intelligence (AI) in Medical Devices: Webinar | Fact Sheet
Chemical Analysis for Biocompatibility Assessment of Medical Devices Draft Guidance for Industry
ENERGY STAR® Requirements for Medical Imaging Equipment
Creation of IEC 60601-1 4th Edition
IEC 60601-1-2 Ed. 4.1 Overview of Requirements
Medical OEM Wireless Coexistence Testing
Biocompatibility Risk Assessment and Evaluation Plans
For more expert papers, recordings, and presentations, visit our Medical Resources hub.
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** The Intertek legal entities that provide medical device management system certification services (including ISO 13485 and MDSAP) and Notified Body services (MDR 2017/745 and MDD 93/42/EEC) do not provide any consulting services. Clients who have used other Intertek legal entities’ consulting services are not eligible to receive management system certification services or Notified Body services from Intertek.