Medical Device Adverse Event Reporting Systems in EU, Canada and US is a webinar that covers topics such as:
- 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
Medical Device Adverse Event Reporting Systems in EU, Canada and US brings together:
- 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
