The Cutting Edge of Medical Technology Content, Community & Collaboration
Wednesday, March 5, 2014
-
Best Practices for Implementing an Adverse Event Reporting System for Medical Devices Including IVDs
March 5, 2014 from 10am to 11am – Online Event This training on Medical Device Reporting (MDR) requirements will provide attendees the best practices for implementing an adverse event reporting system for medical devices including in vitro diagno… Organized by ComplianceOnline | Type: medical
-
Webinar On - Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 Requirements
March 5, 2014 from 12pm to 1pm – Online This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device and pharma companies, many going back to insuffic… Organized by compliancetrainings | Type: online, webinar
MedTechIQ VideoLibrary
Upcoming Events
© 2024 Created by CC-Conrad Clyburn-MedForeSight.
Powered by
