In this webinar, you will learn how to perform searches of the FDA databases for known use errors.
Known Use Errors Search Webinar ($129)
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What You Will Learn in the Known Use Errors Search Webinar:
In this webinar, you will learn how to perform searches of the FDA databases for known use errors. You will also learn how to fill in our template for documenting these known use errors. A work instruction explaining the step-by-step search process is also included in this bundle. This webinar training will be hosted live on our Streamyard platform.
When is the Known Use Errors Search Webinar?
This webinar will be hosted live on Thursday, September 19, 2024 @ 10:30 a.m. ET. If you are unavailable for the live presentation, the session will be recorded an you can download the recording and watch the training as often as you wish.
What you will receive
A Recording of the live webinar as well as:
Other Usability Engineering / Human Factors Training
- Formative Usability Testing Webinar & Template Bundle – $79
- Use Error and Abnormal Use Decision Tree Training – $79
- Use Specification Template & Webinar Bundle – $79
- Task Analysis Template & Webinar Bundle – $129 – Live Webinar, October 17, 2024
- Use-Related Risk Analysis (URRA) Template & Webinar Bundle – $299
- Participant Screening & Data Collection Forms – $79 – November 27, 2024
- Summative Usability Testing Protocol & Webinar Bundle – $199 – Live Webinar, December 19, 2024
- Summative Usability Testing Report – Live-streaming Free Webinar, December 20, 2024
About Your Instructor
Rob Packard is a regulatory consultant with ~25 years of experience in the medical device, pharmaceutical, and biotechnology industries. He is a graduate of UConn in Chemical Engineering. Rob was a senior manager at several medical device companies—including the President/CEO of a laparoscopic imaging company. His Quality Management System expertise covers all aspects of developing, training, implementing, and maintaining ISO 13485 and ISO 14971 certifications. From 2009 to 2012, he was a lead auditor and instructor for one of the largest Notified Bodies. Rob’s specialty is regulatory submissions for high-risk medical devices, such as implants and drug/device combination products for CE marking applications, Canadian medical device applications, and 510(k) submissions. The most favorite part of his job is training others. He can be reached via phone at 802.281.4381 or by email. You can also follow him on YouTube, LinkedIn, or Twitter.