Medical Device Risk Analysis in the Design Process

  • Speaker:Charles H. Paul
  • Duration:60Min
  • Product Code:GRC-90398

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Recorded Session - How it works

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Training CD - How it works

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(For more information about our products contact +1- 248-233-2049)

If you are unable to attend the meeting Live then you can opt in for the Live Recording instead. Access the Recording of the Training for 6 months. Contact our support for any questions. To prepare an invoice to pay by Check or Wire email us at support@grcts.com. 


Certification: GRCTS Attendance Certificate

Background:

Medical Devices by their very nature must be safe for human use and must meet the requirements for which they have been designed.  The process which identifies the risks associated with a medical device that could make the device unsafe or not function as intended is called Risk/Hazard Analysis.

21 CFR Section 820 requires that comprehensive risk analysis be performed as part of the medical device regulatory submissions process and throughout the product’s lifecycle.  ISO 14971 is the risk management standard for medical devices. Its purpose is to help manufacturers establish a risk management process that can be used to identify hazards, estimate and evaluate risks, and develop, implement, and monitor the effectiveness of risk control measures.

This webinar will discuss both the regulatory requirements and the process for conducting effective Risk/Hazard Analysis. 

Why you must attend:

The secret to preventing medical device recalls or at least to minimizing their impact is sound Risk/Hazard Analysis.  Aside from being required, it is absolutely essential and necessary to the development and fielding of medical devices that offer a significant level of protection for patients and manufacturers alike. 

The webinar will explore the basic principles of risk management and planning as they relate to medical device design and as required by the FDA.  It will present a logical process for risk management from risk identification through evaluation/rating and mitigation.

The tools and techniques of Risk Analysis and the rating process used to evaluate the risks identified will be presented and discussed – Fault Tree Analysis, Failure Mode Effects Analysis, and Failure Mode Effects and Criticality Analysis. 

Areas will be talking about:

  • Why Risk/Hazard Analysis is important
  • Risk Assessment Defined
  • Regulatory Requirements
  • Risk Management Process – The Risk Management Plan
  • Risk Management Documentation
  • Risk Analysis Processes and Techniques
  • Asking the Right Questions
  • The Evaluation/Analysis Tools – FTA, FMEA, and FMECA
  • Risk Control/Mitigation

Who will benefit:

  • Quality
  • Production
  • Compliance
  • Engineering
  • R & D
  • Management – essentially everyone in the organization that is involved in the design and development of Medical Devices.
  • It is particularly suited for the health sciences where much project-based work is accomplished.
  • Medical device manufacturers
  • Pharmaceutical and Biotech organizations
  • Cosmetic and foods manufacturers
  • All other related Industries

Instructor:

Charles H. Paul is the President of C. H. Paul Consulting, Inc. – a regulatory, training, and technical documentation consulting firm.  Charles has been a regulatory consultant for over 20 years and has published numerous white papers on the subject.  The firm works with both domestic and international clients designing solutions for complex training and documentation issues.

Available Options

5 Member Group: 5 people can Attend the Live Online Meeting from any location globally

$2,659

10 Member Group: 10 people can Attend the Live Online Meeting from any location globally

$4,679

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