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A Comprehensive View of FDA Regulations for Medical Devices

ComplianceOnline

Thursday, July 20, 2017 at 8:30 AM - Friday, July 21, 2017 at 4:00 PM (EDT)

A Comprehensive View of FDA Regulations for Medical Dev...

Ticket Information

Ticket Type Sales End Price Fee Quantity
Seminar One Registration (Early Bird Price)
Registrations after June 30, 2017 - $1899
Jul 20, 2017 $1,499.00 $0.00
Seminar One Registration Jul 20, 2017 $1,899.00 $0.00

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Event Details

Course 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
  • Teach the current device marketing regulations
  • Discuss how to handle FDA inspections and effectively respond to inspectional observations and 483s


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
  • Learn about correcting devices already shipped and when to report to FDA
  • Learn the role of FDA Inspections, the use of QSIT, and the possible outcomes of an inspection
  • Learn about inspectional observations and how to respond to a Form 483
  • Understand the issues manufacturers face by reviewing Warning Letters related to the topics covered


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
  • R&D engineers


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


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

Have questions about A Comprehensive View of FDA Regulations for Medical Devices? Contact ComplianceOnline

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When & Where


Boston

Boston, MA

Thursday, July 20, 2017 at 8:30 AM - Friday, July 21, 2017 at 4:00 PM (EDT)


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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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A Comprehensive View of FDA Regulations for Medical Devices
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