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Implementing UDI (Unique Device Identification) - Plan Now for Success: One Day In-Person Seminar

ComplianceOnline

Monday, September 9, 2019 from 8:30 AM to 4:30 PM (EDT)

Implementing UDI (Unique Device Identification) - Plan...

Ticket Information

Ticket Type Sales End Price Fee Quantity
Seminar One Registration   more info Ended $999.00 $0.00
Special Group Discount Register for Four attendees Sep 9, 2019 $1,199.00 $0.00

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Event Details

Course Description:

The one-day workshop provides the information you need to implement UDI. An effective implementation gives your customers the information they need. It will also help you avoid an FDA 483 and a Warning Letter.

The workshop gives you hands on experience to understand UDI and your device. You bring a laptop computer and some information about your device. During the seminar you receive toolkits to determine the compliance dates, packaging configurations, and the attributes you will load to GUDID

The workshop helps you identify the requirements for the UDI elements:

  • Procedure changes
  • Label UDI
  • Package UDI
  • Direct marking UDI
  • Date format
  • Entry into GUDID

The workshop helps you implement the changes, update your procedures, and determine when you need to revalidate databases.

 

Who will Benefit:

  • Regulatory Managers
  • Design Engineers
  • Labeling Specialists
  • Project Managers
  • Quality Managers
  • Quality Engineers
  • Executive management
  • R&D staff
  • Strategic planning staff

 

Topic Background:

All medical devices marketed in the US, with limited exceptions, must have unique device identification. The first phase is the revised regulations with an effective date of Dec. 23, 2013.

The subsequent phases depend on device attributes such as regulatory class, intended use (life sustaining or life supporting), reusable & reprocessed, etc. FDA-CDRH published a simple table, by compliance date. However, device manufacturers need a more refined analysis to classify their products and determine the compliance dates.

For each compliance date, depending on the device characteristics, the manufacturer puts the UDI on the label, changes the label’s date format, includes the UDI on packaging configurations, and enters information into the FDA-CDRH database called the GUDID. In some case, the manufacturer puts the UDI on the device itself.

By September 24, 2016, all manufacturers of Class 2 devices must implement UDI (label, package, and GUDID). You need to understand the regulation and develop your plans now or you won’t be ready. There are a lot of details in the implementation and you will need time to handle all of them.

You need to plan your implementation. You have only two choices.

  • You could assign somebody as the subject matter expert. This means reading and understanding the 160 page final rule as well as the ever changing guidance documents
  • You could send your implementation team to this workshop designed to clarify the requirements and provide hand-on practice in the implementation

For Registration : https://www.complianceonline.com/medical-device-udi-implementation-seminar-training-80303SEM-prdsm?channel=eventbrite 

 

 

Note: Use coupon code < REFERRAL10 > and get 10% off 

Have questions about Implementing UDI (Unique Device Identification) - Plan Now for Success: One Day In-Person Seminar? Contact ComplianceOnline

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When & Where


Cambria Hotel Cleveland Avon
35600 Detroit Road
Avon, OH 44011

Monday, September 9, 2019 from 8:30 AM to 4:30 PM (EDT)


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Organizer

ComplianceOnline

At ComplianceOnline, we are focused on:

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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