Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel 2012
06 Jun 2012
Webinar
Key Topics
Subject Areas covered
Valuable documents that provide understanding
QSR Preamble
Quality System Regulation (QSR), including the definitions
FDA`s Quality System Inspection Technique (QSIT) manual
ISO 13485:2003
Warning Letters
Organization
Quality policy
Resources
Responsibility and authority
Management review
Management Representative
Quality system procedures
Quality planning
Who should Attend
Device company Managers, Device Company Executives, Regulatory Affairs Managers, Quality Managers, Management Representatives, Risk Managers, Design Engineering Managers and Production Managers.
Past Events
Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel 2012 - 06 Jun 2012, Webinar (29933)
Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel 2026
Important
Please, check "Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
