The Value of a Human Factors Program

This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

Speaker: Thomas Bento | View Anytime | Price: ¤190.00 | View Details

Validation of Non-Product Software

This course will teach how to comply to 21 CFR Part 820.70(i) and effectively implement a software validation program for medical devices, meeting the FDA requirements and produce a safe product. We will explain the role of Risk Management in Non-Product Validation. How software requirements are used in validation will be described.

Speaker: Thomas Bento | View Anytime | Price: ¤190.00 | View Details

The Value of a Human Factors Program

This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.

Speaker: Thomas Bento | View Anytime | Duration: 60 Minutes | Price: ¤190.00 | View Details