The 3rd Boston Medical Affairs Seminar 2018 is dedicated to the product development road map from early research, approval, launch, and finally to lifecycle.
Topics
- Medical Affairs supporting the regulatory process and building up to Product Approval
- Medical Affairs in early R&D - engaging early and demonstrating value
- Medical Affairs playing a central role in Product Lifecycle Management
- Medical Affairs delivering on goals to support a successful Product Launch
Who should Attend
Professionals with responsibilities in:
- Field Medical/Medical Science Liaisons
- Medical Affairs/Field Medical Affairs
- Medical/Scientific Communications
- Clinical/Scientific Affairs
- KOL/Thought Leadership Relationships
- Clinical Project Management
- Investigator-Initiated/ Sponsored Trials (IITs/ ISTs)
- Health Economics and Outcomes Research
- Compliance/Legal
- Research and Development
- Scientific Engagements
- Quality Assurance
- Telemedicine
- Publication Planning
- Research Collaboration
- Information Management
- Research Grants
- Clinical Trial Monitoring
- Regulatory Affairs
- Clinical Outcomes and Publications
