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Tips for Implementing FDA UDI without Derailing Production
Experts share advice on improving patient safety with Unique Device Identification without throwing your organization off track  Benefits of this webinar: regulations standards complexities of FDA UDI regulations The FDA’s mandate for UDI (Unique Device Identification) for medical devices offers a way of presenting information in a standard format or barcode, making trade, distribution and usage more secure. Compliance, however, can prove to be a time-consuming process, and if done incorrectly, can expose your company to serious setbacks. Aligning yourself with the FDA UDI regulations will impact many areas within your organization and will involve changes to current products and procedures, including required elements in label design, necessary software and hardware and the uptake of barcode standards. In this 60-minute, information-packed session, PRISYM ID was joined by industry experts Jay Crowley, FDA, and Janice Kite, GS1 Global Office, and gave an in-depth look into how to plan and implement UDI strategy with minimal impact on organizations. To view this webinar you must Login or Register first If you would like to submit any questions with regards to this webinar or for more general information contact PRISYM ID Marketing:
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