Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance 2018
14 Feb 2018
Webinar
Description
Topics
Key U.S. FDA Publications that Address UDI Requirements for Regulated Companies
Basic requirements of UDI Labeling and its Database, GUDID
Required steps for UDI / GUDID compliance by the Medical Device Company
UDI / GUDID Implementation Schedules
Future Requirements
Who should Attend
QA/RA
Senior Management in Devices and Combination Products
Marketing
R&D and Engineering
Others Tasked with Product
Consultants
Validations
Process
CROs and Clinicals Personnel
CGMP Responsibilities
Staff and Office Personnel
Medical Personnel
Other Healthcare Professionals
Past Events
Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance 2018 - 14 Feb 2018, Webinar (72923)
Important
Please, check "Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance" official website for possible changes, before making any traveling arrangements
