Impact and Implementation: Alere's VP for Regulatory Affairs on the US FDA Unique Device Identification System

Simon Richards
Contributor: Simon Richards
Posted: 02/20/2014

Ahead of the UDIs and Traceability for Medical Devices Forum 2014, Simon Richards, VP for Regulatory Affairs, EME at Alere, joins Andrea Charles from Pharma IQ to discuss the benefits of a well-built unique device identification (UDI) system, developing a strategy for implementation and future perspectives for medical device manufacturers.

To continue viewing this content please fill out the form below and become an Pharma IQ member.
Or if you're already a Pharma IQ member, sign in below to download.
Join

By entering in your information and submitting the form, you give the sponsor permission to contact you regarding their product and you agree to our User Agreement, Privacy Policy, and Cookie Policy.

Simon Richards
Contributor: Simon Richards
Posted: 02/20/2014

EVENTS OF INTEREST

London, UK
November 27 - 28, 2017
Vienna Marriott Hotel, Vienna, Austria
November 26 - 28, 2017
Hilton Brussels Grand Place, Brussels, Belgium
November 27 - 29, 2017