Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance 2018 is a webinar that covers topics such as:
- 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
Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance 2018 is intended for:
- 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
