Update on Global UDI Initiatives for Medical Devices
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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
OverviewThis 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 AttendKnowledge, 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 WebinarIntent of Unique Device Identification regulations Why are countries creating regulation for UDI?What is the purpose of the regulation?Current efforts & hurdles to harmonizationKey differences in proposed regulationsStandardsLabel requirementsData reportingComparison of IMDRF/ US FDA/ EUTimelines – known & anticipatedImpact of UDI on global trade & commerce, product cost, and patient safetyEnforcement actionsLearning ObjectivesBe aware of what UDI information to look for and where to find itBe able to outline a general UDI strategy by identifying and prioritizing the “critical to business” regulations you need to address firstWho Will BenefitRegulatory Affairs ProfessionalsQuality Assurance ProfessionalsLabeling SpecialistsMaster Data ManagersSupply Chain ProfessionalsFor more detail please click on this below link:http://bit.ly/2rzsp5LEmail: referralscomplianceglobal.usToll Free: +1-844-746-4244Tel: +1-516-900-5515Fax: +1-516-900-5510
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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