Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance 2018

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