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DTSTART:19700308T020000
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UID:2140535:Event:70028
DTSTAMP:20260412T020107Z
SUMMARY:Online Webinar on Update on Unique Device Identifier for Devic
 e Manufacturers
DESCRIPTION:Overview: Recent reports identified several potential bene
 fits to widespread use of UDI, such as reducing medical errors, facili
 tating recalls, improving medical device reporting, and identifying in
 compatibility with devices or potential allergic reactions.The reports
  further indicated that many issues have to be addressed prior to succ
 essful implementation of UDI for devices, including determining the te
 chnology needed to utilize UDI effectively, identifying the data neede
 d for patient safety; development, maintenance, and validation of a ce
 ntral data repository; and harmonizing UDIs for the international mark
 etplace.\nWhy should you attend: Understand how the use of a unique de
 vice identification (UDI) system may improve patient safety, e.g., by 
 reducing medical errors, facilitating device recalls, and improving me
 dical device adverse event reporting. Understand some of the issues as
 sociated with the use of various automatic identification technologies
 .\nAreas Covered in the Session:Understand how to implement the Unique
  Device IdentificationIdentify the uses and benefits of UDIsUnderstand
  the challenges, recommendations and proposed conclusions from multipl
 e groupsReview examples of Device Identification management scenarios 
 reflecting the benefitsLearn where the use of medical device identific
 ation encompasses four current main elements\nWho Will Benefit: This w
 ebinar will provide a general overview and update to companies who nee
 d to better understand industry's and FDA's current overview of Unique
  Device Identification. The employees who will benefit include:All end
 -users from appropriate departments who desire or require a better und
 erstanding and overview of Unique Device Identification and current up
 date.QA and ComplianceRegulatory Affairs and RA SpecialistsMarketingCo
 nsultantsTechnical Writers and employees who review labeling/tracking 
 info\nSpeaker Profile:David R. Dills , Regulatory Affairs & Compliance
  Consultant currently provides regulatory, compliance and quality cons
 ultative services for medical device and pharmaceutical/combination ma
 nufacturers, and also has an accomplished record with more than 24 yea
 rs of experience with Class I/II/III medical devices, In Vitro diagnos
 tics, and pharmaceuticals in the areas of Regulatory Affairs, Complian
 ce and Quality Systems. He has been previously employed, with increasi
 ng responsibilities by medical device manufacturers and consultancies,
  including a globally recognized CRO.\nContact Detail:Compliance4All D
 BA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.comh
 ttp://www.compliance4all.com/Event Link : http://bit.ly/Device_Manufa
 cturersLinkedIn Like usTwitter Follow usFacebook Like us\n\nFor more i
 nformation visit https://medtechiq.ning.com/events/online-webinar-on-u
 pdate-on-unique-device-identifier-for-device
DTSTART;TZID=America/New_York:20160630T100000
DTEND;TZID=America/New_York:20160630T113000
CATEGORIES:webinar
LOCATION:Online Event
WEBSITE:http://www.compliance4all.com/
URL:http://www.compliance4all.com/
CONTACT:8004479407
ORGANIZER;CN="Adam Fleming":https://medtechiq.ning.com/profile/Complia
 nce4all
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562012364?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
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