Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Learn how to design a Human Factors plan using a simple medical device that could be used to satisfy IEC 62366 and other FDA guidance on product development process requirements. From the marketing requirements to the product release, see which Human Factors tasks are integrated and how into the various product development stages.
Webinar was originally aired on Aug 4, 2015. Please fill out the form below to view the recording and access answers to frequently asked questions on Human Factors and FDA compliance.