Medical Device Adverse Event Reporting Systems in EU, Canada and US - Webinar By GlobalCompliancePanel 2012
30 Aug 2012
Webinar
Description
Topics
Definitions
Applicable and relevant regulations in EU, Canada and US
Medical device vigilance system during the post-production phase in EU
Medical device adverse event reporting requirements in EU, Canada and US
Mandatory medical device reporting requirements in US
Mandatory medical device problem reporting requirements in Canada
Applicable and relevant guidance documents
Review of actual reporting forms in EU, Canada and US
Who should Attend
Clinical Affairs Managers, Directors and VPs
Regulatory Affairs Managers, Directors and VPs
Quality Managers, Directors and VPs
Quality Managers, Directors and VPs
Sales and Marketing Managers, Directors, and VPs
Compliance Managers and Directors
Site Managers, Directors, and Consultants
Complaint Handling and Risk Management Managers and Directors
Compliance Officers and Legal Counsel
Senior and Executive Management
Business Development Managers, Directors, and VPs
Past Events
Medical Device Adverse Event Reporting Systems in EU, Canada and US - Webinar By GlobalCompliancePanel 2012 - 30 Aug 2012, Webinar (31884)
Important
Please, check "Medical Device Adverse Event Reporting Systems in EU, Canada and US - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
