New EU Pharmacovigilance Directive and Regulations 2013 is a webinar that covers topics such as:
- EU Pharmacovigilance : Why make changes now?
- Overview of EU Regulatory structure
- Organization of PV Modules
- New definitions for the updated directive and regulation
- Eudravigilance Database
- Update to the EU Pharmacovigilance legislation
- The Pharmacovigilance Risk Assessment Committee
- Changes to labeling
- Implementation timing & expectations
New EU Pharmacovigilance Directive and Regulations 2013 brings together:
- Project Managers
- Senior Management
- PV Reporting
- Clinical Trial Heads
- Project Managers
- Medical Writers
- QA / Compliance personnel
- CRAs and CRCs
- Clinical Research Scientists
- Investigators
- Consultants
- QA / QC Auditors and Staff