9th REMS Summit - Arlington, VA

9th REMS Summit
January 26 - 27, 2017
Arlington, VA
Arlington, VA

Sharing Information and Best Practices on Regulatory Changes, Emerging Technologies and Trends, and Tools to Ensure Patient Safety and Compliance

9th REMS Summit – 9th REMS Summit

In light of our marked success last year, the REMS Summit will again convene stakeholders to inform the design and redesign of REMS programs. Attendees will learn how to integrate with healthcare systems by talking with healthcare providers, pharmacists and patient advocates about the particular burdens that REMS imposes on them. In addition, they will synthesize the impact of REMS programs on stakeholders, new and pending FDA regulations, available resources, and trends to institute conditions essential for safe drug use and REMS compliance. Participants will learn key methods for implementing, executing, assessing and modifying REMS, including leveraging strategic partnerships, instituting adaptive internal structures and streamlining processes.

The insights of a broad array stakeholders are complemented by the comprehensive elucidation of information and strategies. The 9th REMS Summit will feature sessions on research-based risk management strategies and poignant lessons from Implementation Science. Attendees will be presented with proven methods and vetted technologies to adopt and/or adapt to bolster the efficacy of their REMS programs. This series continues to be the preeminent event for updates related to new regulations and emerging REMS issues, including standardization, evaluation and structured product labeling.

Learn from and interact with your peers as well as crucial stakeholders and preeminent thinkers who comprise our speaking faculty.

We welcome you to witness firsthand why our event remains the conference of choice for REMS professionals.

Top Five Reasons to Attend

  1. Learn best practices in facilitating benefit-risk counseling between patients and providers
  2. Determine solutions to integrate REMS with healthcare systems and pharmacies
  3. Adapt an app or other technology as a viable medium for REMS
  4. Institute best practices for evaluating patient safety and patient outcomes
  5. Tailor strategies and communications to inform and engage stakeholders with disparate needs

Who Should Attend

This conference is designed for professionals from pharmaceutical and biotechnology companies with responsibilities in the following areas:

  • REMS
  • Risk Management
  • Pharmacovigilance/Surveillance
  • Medical Director
  • Quality Assurance
  • Drug/Product Safety
  • Clinical Risk Management
  • Life Cycle Management
  • Regulatory Affairs/Legal/Compliance
  • Clinical Affairs
  • Clinical Data Management
  • Clinical Operations
  • Clinical Risk Management Compliance
  • Epidemiology/Pharmacoepidemiology
  • Marketing

This event is also of interest to:

  • Risk Safety and REMS Service Providers
  • Data Management Service Providers
  • Consultancies
  • Dashboard and Metrics Service Providers
  • Law Firms
  • Healthcare Information Marketing and Technology Providers
live chat software