The Validation of Non Product Software

By: Thomas Bento ,Sr. Regulatory Consultant.

How to comply with 21 CFR Part 820.70(i) and effectively implement a software validation

  • 05-December-2019| 03:00 PM ET | 12:00 PM PT | 02:00 PM CT Duration 60 Minutes

Navigating the 510(k) process

By: Thomas Bento ,Sr. Regulatory Consultant.

Simplified defensible approach to a successful submission

  • 12-November-2019| 12:00 PM ET | 09:00 AM PT | 11:00 AM CT Duration 60 Minutes

The Value of Human Factors

By: Thomas Bento ,Sr. Regulatory Consultant.

The ISO 62366 is noted by FDA as a “Consensus” Standard, making it a gold standard

  • 22-October-2019| 11:00 AM ET | 08:00 AM PT | 10:00 AM CT Duration 60 Minutes
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