What is the process of registering with 247compliance.com webinars?

You can register for our events and webinars through a simple registration process. Choose a program of your choice and fill in a simple, hassle-free registration form to get started.

Is there an option of purchasing a recorded webinar?

Yes. Besides purchase of live webinar sessions, you can also make a purchase of recorded webinars.

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Your online transactions with us are extremely secure. We operate on a safe and reliable platform and hence your data is safeguarded from misuse, unauthorized disclosure or access, destruction, modification or loss.

A webinar is a live meeting that takes place over the web. The meeting can be a presentation, discussion, demonstration, or instructional session. Participants can view documents and applications via their computers, while shared audio allows for presentation and discussion.

What is a recorded session?

Recorded audio and video of a WebEx session alone with presentation where the speaker explains his area of expertise (Note: This does not include the live session)

How long does an average webinar span?

The duration of an average webinar extends anywhere between 60 minutes to 90 minutes.

How do I receive confirmation of my registration?

Upon registration, you will receive confirmation intimation through email. At the end of the registration process, we will send you an invoice letter.

Edwin Waldbusser - trainingspoint.com

Edwin Waldbusser, is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the areas of design control, risk analysis and software validation for the past 8 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.

Edwin Waldbusser

LIVE WEBINARS

21 CFR Part 11 - Compliance for Electronic Records and Signatures

FDA Regulation of Artificial Intelligence/ Machine Learning

RECORDED SESSIONS

21 CFR Part 11 Conformance for Medical Devices

Software Validation for the New FDA Inspections

Medical Device Hazard analysis following ISO 14971

Human Factors Usability Studies Following ISO 62366 and FDA Guidance

How to Prepare For and Host a FDA Inspection and Respond to 483's