Risk Communication of Medical Device Failures

Speaker

Instructor: Marta L Villarraga
Product ID: 700450

Location
  • Duration: 60 Min
This Risk communication webinar/training will review the types of risk communications that take place regarding medical device failures at both pre- and post-marketing stages in the lifecycle of medical devices.
RECORDED TRAINING
Last Recorded Date: Aug-2007

 

$249.00
1 Person Unlimited viewing for 6 month info Recorded Link and Ref. material will be available in My CO Section
(For multiple locations contact Customer Care)

$500.00
Downloadable file is for usage in one location only. info Downloadable link along with the materials will be emailed within 2 business days
(For multiple locations contact Customer Care)

 

 

Customer Care

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Email: [email protected]

Read Frequently Asked Questions

 

Risk communication of medical device failures can take place at both the development (pre-marketing) and post-development (post-marketing) stages of any medical device. Identifying medical device failures and communicating these findings are essential components during both stages. Effective risk communication of medical device failures provides manufacturers with the appropriate information to make decisions regarding the risks to health, patients, and overall safety. It also provides the public (end-users and patients) with increased knowledge on the performance of medical devices, their use in medical procedures and the potentials for malfunction, misuse, or hazards.

Areas Covered in the seminar:

  • Why is risk communication important?
  • What is the role of risk communication within risk management?
  • How risk communication is different before and after a product has been released to the market?
  • What is important in risk communication before the product has been released to the market?
  • What is the role of risk communication after the product has been released to the market?

Who will benefit:

This presentation will review the types of risk communications that take place regarding medical device failures at both pre- and post-marketing stages in the lifecycle of medical devices. The employees who will benefit include:

  • Engineering staff in design and manufacturing
  • Health professionals who interface with physician or patient users
  • QA managers and personnel
  • Regulatory Affairs managers and personnel

Instructor Profile:

Marta L. Villarraga,: Ph.D. is a Principal Engineer at Exponent, Inc, a scientific and engineering consulting firm. Dr. Villarraga concentrates her practice in failure analysis of medical devices in the areas of product liability, intellectual property, regulatory compliance, quality control and manufacturing compliance. She has assisted companies with root cause analyses prior to a recall or as part of the investigation following a recall being announced. Dr. Villarraga is also a reviewer for various scientific journals. She has also published a number of scientific articles and frequently presents at national conferences. She recently contributed to various chapters in the book "Bringing your Medical Device to Market," including one on medical device recalls. She also holds adjunct faculty appointments at various local and regional universities where she often lectures.

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Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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