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Deviation Management System 2013
29 Jan 2013
Webinar
Home
Deviation Management System 2013
Description
Topics
EU Requirements
FDA Requirements
Elements of the Investigation Process
Landmark Case
Root Cause Analysis Techniques
Skills and Tools of the Investigator
CAPA
Who should Attend
Quality Assurance
Investigators
Complaints Manager
Laboratory Supervisors
Quality Assurance
CAPA Manager
Past Events
Deviation Management System 2013 - 29 Jan 2013, Webinar
(32794)
Important
Please, check "Deviation Management System" official website for possible changes, before making any traveling arrangements
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