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Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-day In-person Seminar

ComplianceOnline

Thursday, December 15, 2016 at 8:30 AM - Friday, December 16, 2016 at 4:30 PM (MST)

Medical Device Risk Management A to Z - Best Practices...

Ticket Information

Ticket Type Sales End Price Fee Quantity
Seminar One Registration (Early bird price)
For Registrations after November 25, 2016 - $1999
Dec 15, 2016 $1,699.00 $0.00
Seminar One Registration Dec 15, 2016 $1,999.00 $0.00

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Event Details

Course Description:

The course is designed for Medical Products Manufacturers. The course will be taught for Medical Devices and Combination Products, but will also be of benefit to Pharmaceutical Manufacturers. 

Learning Objectives:

Upon completion of the course, the participants will have learned how to implement good risk management principles into medical products manufacturing operations such as medical devices, combination products, and pharmaceuticals:

  • Understand what are the current issues and recommended solutions
  • How to implement the ISO 14971 framework
  • Use a Traceability Report for improved risk management operations
  • How to Use Standards to Facilitate Product-to-Market Achievements
  • How to Use Risk Management to Identify the Critical Success Factors
  • Key implementation issues related to Risk Management
  • Using Risk Management to identify key opportunities for the organization
  • Risk Integration Issues, especially related to the Quality System and Design Controls
  • Use of appropriate risk management tools beyond FMEA

 

Who will benefit:

The course is designed for manufacturing professional employees that must interface with or implement product risk management activities in a medical product manufacturing operation.

  • Product Risk Managers
  • Quality Assurance
  • Regulatory Affairs
  • Research & Development
  • Project Managers
  • Operations Managers
  • Manufacturing Managers
  • Engineers

 

For Registration -  http://www.complianceonline.com/iso-14971-medical-device-risk-management-a-to-z-best-practices-seminar-training-80076SEM-prdsm?channel=eventbrite         

 

Note: Use coupon code NB5SQH8N and get 10% off on registration.

Have questions about Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-day In-person Seminar? Contact ComplianceOnline

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When & Where


Salt Lake City

Salt Lake City, UT

Thursday, December 15, 2016 at 8:30 AM - Friday, December 16, 2016 at 4:30 PM (MST)


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Organizer

ComplianceOnline

Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.

Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.

Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.

Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.

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Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-day In-person Seminar
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