A Comprehensive View of FDA Regulations for Medical Devices

Expired
Dates : 11 June 2016 » 12 June 2016

Place : Boston
United States

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Organizer :

Engineering and Technology;
Keywords: Design, Manufacturing
Description :

Don’t let a common misunderstanding get you into trouble! There is more to the US Medical Device Regulations than Part 820.

Companies that don’t understand will face regulatory scrutiny and receive FDA Form 483s and Warning Letters. Recently a device manufacturer got a Warning Letter relating to updates to shipped devices, which said, “The Quality Manager stated he was unaware of the corrections and removal reporting and recordkeeping requirements.”

This two day interactive course on FDA regulations for medical devices will:

  • Cover more than just the Quality Management System
  • Provide an overview of regulations and how they fit together
  • Explain Unique Device Identification (UDI) in detail, covering the issues device manufacturers will face as well as timeline for implementation
  • Help attendees understand the four major elements of the US regulatory structure: laws, regulations, guidance, and consensus standards
Learning Objectives:
  • Learn the law, regulations, and policies that FDA applies for medical device
  • Understand the requirements to market a medical device in the US including device classification and conformity assessment paths
  • Understand the quality management systems that govern the design, manufacture, installation, and servicing of medical devices for the US market
  • Learn how UDI will affect medical devices and how to prepare for implementation
  • Understand the rules for Medical Device Reports (MDRs) and their relationship to complaints
  • Understand which devices must be tracked and how to set up and audit the system
Who will Benefit:

This seminar course will be beneficial for the following personnel in medical device manufacturing companies and in medical device supply chain:

  • Quality managers
  • Quality engineers
  • Quality assurance and quality control
  • Regulatory affairs managers
  • Regulatory affairs professionals
  • R&D managers

 

Note:

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

 

For Registration:

http://www.complianceonline.com/fda-regulations-for-medical-devices-seminar-training-80118SEM-prdsm?channel=sciencedz 


A Comprehensive View of FDA Regulations for Medical Devices to be held from 11 June 2016 to 12 June 2016 in Boston, United States. It covers various areas of Biology and life sciences including . For more information, visit the website of the conference or contact the organizer.
Add to calendar 2016-06-11 2016-06-12 Europe/London A Comprehensive View of FDA Regulations for Medical Devices https://www.sciencedz.net/en/conference/19925-a-comprehensive-view-of-fda-regulations-for-medical-devices Boston - United States

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