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How To Implement Risk Management in Medical Devices Industry: 3-day In-Pers...

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Location

Hilton Zurich Airport

Hohenbühlstrasse 10

8152 Opfikon

8152 Zurich

Switzerland

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Refund Policy

Refunds up to 30 days before event

Eventbrite's fee is nonrefundable.

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Description

Applying ISO14971 / IEC62304 / IEC62366-1 - A Practical Guide On How To Implement Risk Management: 3-day In-Person Seminar, taking place on November 4-6, 2019 at Hilton Zurich Airport.
Risk management is a mandatory and necessary process during the entire device life. Not only will it help to design and maintain devices efficiently, but it also ensures that the device will be as safe as possible and prevents harms to patients, users, and the environment.

Like any process that tries to produce repeatable and consistent results, the risk management process must be clearly understood, including the strengths but also the limitations.

By attending this seminar you will learn the main elements of ISO 14971, ISO 13485, IEC62304, IEC62366-1/-2, risk management life cycle steps and benefits, and FDA software reviewers' guidance. (Read more)

Wednesday, September 25 is the last chance to register & save 15% on TOP of Early Bird pricing. Be sure to mention Coupon Code “324770” when checking out to avail flat 15% off..

Register Now => or follow the below link.

https://www.complianceonline.com/applying-iso14971-iec62304-iec62366-1-a-practical-guide-on-how-to-implement-risk-management-80608SEM-prdsm?channel=irshad_eb

Learning Objectives:
Upon completing this course participants should:

  • Understand the risk management process, the activities, and deliverables as well as the organization framework necessary
  • Be able to Interpret and discuss the requirements of ISO 14971
  • Develop a risk analysis framework document
  • Be able to conduct risk analysis team meetings
  • Recognize how and where to use the various techniques during the design life cycle.
  • Understand how to apply ISO 14971 into development process
  • Know how to document your Risk Management
  • Explain how your Risk Management system fits into quality system and business practices.
  • Perform risk assessments effectively

Who will Benefit:

This course is relevant to managers, supervisors, QA / RA, and design/system engineers. Even experienced personnel will benefit from the "across industry" perspective and the illustration of standard practices that only a presenter with extensive experience in more than 100 projects can provide. Specific positions that would benefit are:

  • Senior Quality Managers
  • Quality, Regulatory & Compliance Professionals
  • Project, Risk & Production managers
  • Engineering management
  • Quality Assurance personnel
  • System, Software, Usability and design engineers
  • Verification / validation personnel
  • Quality & Quality Engineers
  • Medical Affairs Professionals

To view the complete agenda, download the brochure.

Register Now =>

Register Now Pay Later: to reserve your seat on 15% discount on TOP of early bird price; valid till October 4, 2019.

Just Fill this Pre-Registration Form (pdf) and email it to us. We will get back to you with your registration confirmation. In case of any change in your schedule, you can cancel or substitute your registration 30 days before the event date.

Please contact me if you like to register for this seminar on discunted price.

Regards,
Mohammad Irshad

D: +1 650-332-0381

Email: Mohammad.Irshad@ComplianceOnline.Com


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Date and Time

Location

Hilton Zurich Airport

Hohenbühlstrasse 10

8152 Opfikon

8152 Zurich

Switzerland

View Map

Refund Policy

Refunds up to 30 days before event

Eventbrite's fee is nonrefundable.

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