Update on Global UDI Initiatives for Medical Devices
WebcastFaculty
OVERVIEW
Update on Global UDI Initiatives for Medical Devices is organized by Compliance Global Inc. and would be held on Jun 21, 2017.
The target audience for this medical event for Regulatory Affairs Professionals, Quality Assurance Professionals, Labeling Specialists, Master Data Managers, Supply Chain Professionals. 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.
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.
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.
Additional details will be posted as soon as they are available.
The target audience for this medical event for Regulatory Affairs Professionals, Quality Assurance Professionals, Labeling Specialists, Master Data Managers, Supply Chain Professionals. 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.
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.
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.
Additional details will be posted as soon as they are available.
SPECIALITIES
Healthcare Technology
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