How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel 2011
27 Apr 2011
Webinar
Description
The webinar will cover the following topics:
How to conduct a record audit
DHR audit
FDA warning letters
Major FDA 483 points and issuance prevention
QS regulation
Guidance documents
The event brings together:
Consultants
Regulatory and Compliance Managers
Operations executives
Directors, Managers and vice presidents
Quality assurance executives, engineers and field Auditors
Senior executives from pharmaceutical and medical device companies
Past Events
How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel 2011 - 27 Apr 2011, Webinar (15201)
Important
Please, check "How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Operations, Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Hospitals & Clinics, Medical device, Pharma
