Risk Assessment for Medical Devices

6 years ago Posted By : User Ref No: WURUR24257 0
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  • TypeWebinar
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  • Location Bakersfield, California, United States
  • Price
  • Date 13-08-2018
Risk Assessment for Medical Devices, Bakersfield, California, United States
Webinar Title
Risk Assessment for Medical Devices
Event Type
Webinar
Webinar Date
13-08-2018
Last Date for Applying
13-08-2018
Location
Bakersfield, California, United States
Organization Name / Organize By
247compliance
Organizing/Related Departments
Marketing
Organization Type
Event Management Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Medical/Healthcare/Hospital

Location
Bakersfield, California, United States

OVERVIEW

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 SHOULD YOU 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.


LEARNING OBJECTIVES

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 COVERED

  • 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?

  • Anyone involved in the manufacturer of medical devices that has had some exposure to the subject area and regulated environments.
  • American Society for Quality
  • Medical Device manufacturers Association
  • European Medical Device Technology
  • Gulf Coast Medical Device Manufacturers
  • Medical device manufacturers

 

SPEAKER

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.

Others Details

Time: 01:00 PM EST| 10:00 AM PST

Registration Fees
Available
Registration Fees Details
Live session for single participant $149 online
Registration Ways
Email
Phone
Website
Address/Venue
  online  Pin/Zip Code : 93301
Official Email ID
Contact
Operation Manager

online

[email protected]

   +1-(510)-868-1040