US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

Organizer: 
Meeting Description: 

Learn the basic overview of the original medical device Quality Management System -- The US FDA’s CGMP, Quality System Regulation (QSR) under 21 CFR 820. Implementation, training requirements and content, and annual internal audit / inspection expectations. The FDA’s four key areas of compliance under QSIT.

Specialty: 
Medical Management
Event Venue: 
online event
Venue Street: 
6201 America Center Drive Suite 240
Country: 
United States
State: 
California (CA)
City: 
San Jose
Map: 
United States San Jose (Show on map)
Contact Name: 
Ashutos Swain
Email Address: 
Phone: 
+1-888-717-2436
Event Website: 
https://www.complianceonline.com/us-fda-medical-device-qsr-21-cfr-820-and-quality-management-system-webinar-training-705794-prdw?channel=ptmg
Start Date: 
06/08/2021
Time:
10:00 AM
Finish Date: 
06/08/2021
Time:
1:00 PM
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