Webinar on Update on Unique Device Identifier for Device Manufacturers

MessageThis Webinar is over
Date Jun 30, 2016
Time 10:00 am
Cost $150.00
Online
Overview:  
Recent reports identified several potential benefits to widespread use of UDI, such as reducing medical errors, facilitating recalls, improving medical device reporting, and identifying incompatibility with devices or potential allergic reactions.
The reports further indicated that many issues have to be addressed prior to successful implementation of UDI for devices, including determining the technology needed to utilize UDI effectively, identifying the data needed for patient safety; development, maintenance, and validation of a central data repository; and harmonizing UDIs for the international marketplace.

Why should you attend: 
Understand how the use of a unique device identification (UDI) system may improve patient safety, e.g., by reducing medical errors, facilitating device recalls, and improving medical device adverse event reporting. Understand some of the issues associated with the use of various automatic identification technologies.

Areas Covered in the Session:
Understand how to implement the Unique Device Identification
Identify the uses and benefits of UDIs
Understand the challenges, recommendations and proposed conclusions from multiple groups
Review examples of Device Identification management scenarios reflecting the benefits
Learn where the use of medical device identification encompasses four current main elements

Who Will Benefit: 
This webinar will provide a general overview and update to companies who need 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 understanding and overview of Unique Device Identification and current update.
QA and Compliance
Regulatory Affairs and RA Specialists
Marketing
Consultants
Technical Writers and employees who review labeling/tracking info

Speaker Profile:
David R. Dills , Regulatory Affairs & Compliance Consultant currently provides regulatory, compliance and quality consultative services for medical device and pharmaceutical/combination manufacturers, and also has an accomplished record with more than 24 years of experience with Class I/II/III medical devices, In Vitro diagnostics, and pharmaceuticals in the areas of Regulatory Affairs, Compliance and Quality Systems. He has been previously employed, with increasing responsibilities by medical device manufacturers and consultancies, including a globally recognized CRO.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/Device_Manufacturers
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