Dear colleagues, hello 👋
I want to share with you an exciting announcement.
I have designed a 4h, live hands-on workshop on post-market surveillance of medical devices. I would like to invite you to register for the next session coming soon.
Here are the 5 learning objectives of this workshop:
In this workshop, you will learn by doing! There are 3 hands-on activities to help you practice key concepts:
Analyze trending data on a case study device to detect safety signals
Apply the SNIP method for signal evaluation
Estimate probability of occurrence of harm from post-market data.
Since the initial kick-off in February of 2025, nearly 40 QA/RA/Clinical professionals have participated in this workshop. We are receiving a lot of good feedback, including this one from a recent attendee:
A special offer for subscribers of Let’s Talk Risk!
As a subscriber of the Let’s Talk Risk! newsletter, you can save 20% on regular price ($199) if you register by May 7th.
Don’t worry if you cannot attend your assigned session due to scheduling conflicts. This workshop is conducted live via zoom and offered every other 2-3 weeks. So, you can always attend another one at a future date.
When you pass the final quiz, you will get a certificate of competence like this:
Space is limited to only 10 attendees in each session.
Save your spot today!
Looking forward to meeting you in the workshop!
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