C4A – Medical Device Hazard Analysis Following ISO 14971

When:
April 6, 2021 @ 10:00 am – 11:00 am
2021-04-06T10:00:00-07:00
2021-04-06T11:00:00-07:00
Where:
webinar

https://www.compliance4alllearning.com/webinar/medical-device-hazard-analysis-following-iso-14971-503674LIVE

By Edwin Waldbusser

$150

The US FDA expects that as part of a product development Design Control Program risk management will be conducted. FDA also expects a post production risk management program be implemented. 

Areas Covered in the Session:

  • Explanation of Hazard Analysis terms: hazard, hazardous situation, harm, risk
  • Explanation of the hazard analysis process using a template
  • Examples of terms will be given will be covered step by step
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