'Unique device identification system' presentation slideshows

Modeling the Adoption of Identification Standards in the U.S. Healthcare Supply Chain

511 views • 30 slides

Unique Device Identification

Unique Device Identification. Jay Crowley Senior Advisor for Patient Safety Food and Drug Administration jay.crowley@fda.hhs.gov 301-980-1936. Device Information Lifecycle. GPOs. Clinical Substitution. Rentals. Manufacturer. Distributor. Device X Lot Y Exp Date Z. Sold. Hospital.

229 views • 22 slides

Unique Device Identification

Unique Device Identification. Jay Crowley Senior Advisor for Patient Safety Food and Drug Administration jay.crowley@fda.hhs.gov 301-980-1936. Current Device Identification. Non-standard device identification systems; standards used in different ways Not necessary unique or unambiguous

433 views • 19 slides

Implementing a Unique Device Identification System

This webinar will discuss the regulatory and compliance requirements to implement a system for Unique Device Identification (UDI) including final rules, compliance dates and requirements. The speaker will walk you through the requirements including, but not limited to, what to consider when implementing a UDI system in a proactive, streamlined manner. This seminar is intended to help you effectively implement a unique device identification (UDI) system (UDI system) based on the final rules issued on September 20, 2013 and published in federal register on September 24, 2013. This final rule is effective 90 days after date of publication in the federal register. Specifically, new changes in the final rules will be discussed, contributing to saving an enormous amount of time, efforts and resources to achieve compliance and to remain compliant with the final UDI system requirements.

106 views • 5 slides