Compliance with Clarissa - 2022
Episode 11: “Medical Safety 60601-1 3.2” with Joel Smith
12 December 2022
Episode 10: “FDA 510k Submission Consulting” with Bhavesh Sheth
15 November 2022
Episode 7: “Medical Robots” with Bill Stearns
04 October 2022
Episode 6: “Compliance of Wireless Medical Devices” with Ollie Moyrong
20 September 2022
Episode 5: "Hazardous Chemical Compliance" with Matt Quinn
06 September 2022
Episode 4: "Questions About FDA and MDR" with Chris Wyman
23 August 2022
Episode 1: "Risk Assessments", with Mike Brousseau
13 July 2022

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Chemical Analysis for Biocompatibility Assessment of Medical Devices Draft Guidance for Industry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.