MyMeds&Me join industry & regulatory colleagues at the forthcoming DIA Pharmacovigilance and Risk Management Strategies 2016 event, taking place at the Mandarin Oriental Washington Hilton, DC from 25 – 27 January 2016.
During this three-day meeting, thought leaders from around the world will provide their insights and engage in dialogue on current and potential new opportunities, operational challenges, and practical aspects, as well as demands in managing product risk in the context of benefits, in the ever-changing world of medical product safety, pharmacovigilance, and global regulations.
This event provides a unique opportunity for dialogue with representatives from FDA and other key regulatory agencies, as well as from industry and academia.
- Global Regulatory Safety Updates
- New Data Sources for Safety Assessment
- Current Approaches to Benefit-Risk Assessment
- Luncheon Roundtable Discussions with Key Thought Leaders
Meet members of the MyMeds&Me team in the exhibit hall and check out the latest demonstrations of the Reportum® adverse event and product quality capture solution. We look forward to meeting you and learning more about your plans to transform your pharmacovigilance processes.
More information on the event can be found online at: http://bit.ly/1PqnGXl
Register online at: http://bit.ly/1QPVIrz