Hazard Analysis and Risk Management under ISO

28 Apr 2020

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This webinar will address the procedures, provide and discuss suggested templates, necessary to develop or modify and then use the ISO 14971 and Q9 models to perform and document such activities for any medical product. It will examine the additional actions necessary to make it useful as a product reference, for CAPA, root cause / failure investigation, and validation prioritization, and training tool, and how to maintain it as a “living document”. In this webinar,a field-tested model will be presented which incorporates a Narrative, Hazard Analysis, FTA, three FMECAs, and a Report / Conclusion.


  • Suggested and Field-tested Risk Management File / Report, FMECA, FTA Templates
  • Session on why and how to use the ISO 14971 "Model" in all regulated industries
  • Covers areas like product hazard analysis, fault tree analysis,ICH Q9 for Pharma and others


Starts at 10:00 AM GMT-07:00

Entry Fees

Paid Ticket Starts from 229 USD View Details


100 - 500
Based on previous editions

Category & Type

Science & Research
IT & Technology


28 Apr 2020

Frequency Annual
Next edition likely in Apr 2021

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USA 525 Total Events / 70 Upcoming Events 66+ Followers


John E Lincoln

John E Lincoln

Principal, J E Lincoln and Associates

User Community [ Users who have shown interest for this Event ]

Akilesh Kurunghat

Akilesh Kurunghat

Business Development Executive at Eventorg

Kochi, India

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229 USD LIVE ONLINE TRAINING:-One Dial-in One Attendee
599 USD LIVE ONLINE TRAINING:-Group-Max. 10 Attendees/Location
299 USD RECORDED VERSION:-1x Person - Unlimited viewing for 6 Months

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