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LTR Weekly Digest #27 - 9th March, 2024

Catch up on this week's articles - a benefit-risk webinar recording, integrating risk management with design controls, and a quick tip about building equity in medical device design.

Dear colleagues, hello! 👋

A special welcome to 30+ new members who have joined our Let’s Talk Risk! community in the first week of March! Feel free to browse past articles in the archive section of the Let’s Talk Risk! website, and check out recordings of recent LTR conversations in the podcast section.

Here are links to articles published this week.


Announcements

LTR monthly webinar series: How to create a master harms list using standard codes

A quick reminder to join me in this month’s webinar, where I will review standardized codes and terms, and provide a step by step example of creating a master harms list for a medical device using public data.

If you are a paid subscriber, you will receive an email with a link to register for this month’s webinar on March 26, 2024 at 11:00 AM EST. You don’t need to pay extra.

If not, you can still attend this webinar with a one time payment of only $25. Click the link below to make a payment and secure your spot. Once you complete the payment, you will receive the registration link by email.

Register now to attend (Only $25)


LTR weekly conversation on LinkedIn: 3 MedTech trends to watch in 2024

Join me next Thursday, March 14, 2024 at 11:00 AM EST, for another Let’s Talk Risk! conversation on LinkedIn. My guest this week is Jennifer Mascioli who will discuss 3 MedTech trends risk practitioners should watch in 2024.

Join the conversation!


Pre-registration is now open for the next session of Live ISO 14971 training on ACHIEVE. Paid subscribers get 20% off regular price!

Save your spot here to join the next cohort of the LIVE ISO 14971 certification training course starting in March 2024. Watch a course introduction video and check out testimonials from past attendees!

Pre-register now


Weekly Knowledge Challenge

I hope you enjoyed the knowledge challenge question last week. Here is the correct answer:

The correct answer for the question, “Since it is not explicitly required by ISO 13485:2016, the final rule o QMSR also does not require device manufacturers to inspect labeling and packaging before use.” is False.

Here is this weeks’ knowledge challenge #24

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