EDM, ERS, and RIM have combined for the 2016 Regulatory Submissions, Information, and Document Management Forum. This forum will cover topics in four tracks: Electronic Regulatory Submissions (ERS), Regulatory Information Management (RIM) Business, RIM Technology, and Electronic Document Management (EDM).
The forum is currently being developed. Please continue to check the website for additional information.
Who should attend?
- Regulatory Affairs and Operations
- Regulatory Information Management
- Global Submission Managers/Project Managers
- Medical, Technical, and Regulatory Writers
- Data Managers
- Information Technology and Support Personnel
- Document and eRecords Managers
- Regulatory Standards Implementation Specialists and Associates
- Clinical Operations Representatives
- Quality Assurance and Compliance Professionals
- Contract Researchers and Service Support Providers
- Emerging Pharmaceutical/Biotech/Device Professionals
- Vendor Relationship Managers
More details and registration: