DMR & DHR - What Is Really Required 2012
February 29, 2012(Ended)
Online Webinar
DMR & DHR - What Is Really Required is a webinar that covers topics such as:
- Key Definitions
- The FDA’s QSR
- Quality System Record (QSR)
- Design History File (DHF)
- Device History Record (DHR)
- Device Master Record (DMR)
DMR & DHR - What Is Really Required brings together people involved in design, project management, purchasing, production, servicing, installation, record keeping activities and document control for medical device manufacturing including: Quality Professionals, Quality Managers, Production Managers, Regulatory Professionals, Project Managers, Risk Managers, Manufacturing Engineers, Production Supervisors, Design Engineers, Production Engineers, Quality Engineers, Process Owners, Document Control Specialists, Quality Auditors and Record Retention Specialists.
Prices *
299-1199 US Dollar
Exhibition
No exhibition
Organization
Categories
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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