Update on Global UDI Initiatives for Medical Devices

Website http://bit.ly/2rzsp5L | Edit Freely

Category unique device identification;UDI program

Deadline: June 21, 2017 | Date: June 21, 2017

Venue/Country: New York, U.S.A

Updated: 2017-05-26 19:04:58 (GMT+9)

Call For Papers - CFP

This webinar will provide updates on the progress of unique device identification regulations around the world, including the status of the FDA’s implementation, requirements for UDI in the new EU MDR, the NHS e-procurement and PEPPOL programs in the UK, and the development of initiatives in other countries including Australia, Canada, Japan and Asia.

Unique identification and barcoding are neither new technologies nor innovative concepts. But incorporation of UDI into the medical device industry has been long discussed and planned and slow to be implemented.

What has taken this major industry so long to adopt UDI and barcoding? Why are both manufacturers and hospital systems reticent about implementing it?

Why Should You Attend

Knowledge, planning, preparation. These are the foundation principles for any successful and sustainable project, especially one as global and multi-faceted as Unique Device Identification. It is never too soon to begin increasing your awareness of the various programs being established and your knowledge of the requirements and timelines to help you begin planning and preparing for what is inevitably going to be a challenging, resource-heavy, and time-consuming process.

Medical device manufacturers of all sizes, locations, product class, and expertise are in the same precarious position of uncertainty and waiting. By strengthening your UDI intelligence now, you will be better positioned to lead your organization in this global initiative.

Areas Covered in this Webinar

Intent of Unique Device Identification regulations

Why are countries creating regulation for UDI?

What is the purpose of the regulation?

Current efforts & hurdles to harmonization

Key differences in proposed regulations

Standards

Label requirements

Data reporting

Comparison of IMDRF/ US FDA/ EU

Timelines – known & anticipated

Impact of UDI on global trade & commerce, product cost, and patient safety

Enforcement actions

Learning Objectives

Be aware of what UDI information to look for and where to find it

Be able to outline a general UDI strategy by identifying and prioritizing the “critical to business” regulations you need to address first

Who Will Benefit

Regulatory Affairs Professionals

Quality Assurance Professionals

Labeling Specialists

Master Data Managers

Supply Chain Professionals

For more detail please click on this below link:

http://bit.ly/2rzsp5L

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