8th Risk Evaluation and Mitigation Strategies Summit 2016
ArlingtonArlington, USA Visit the Venue to read more
This summit provides a platform to share best practices on how to design, develop, implement and evaluate REMS. The most experienced professionals from a cross section of small to large companies address major challenges and discuss how they’ve managed to apply lessons learned from various REMS programs.
This event provides an interactive atmosphere to cover REMS from A to Z. Learn from high-level case studies and panel discussions with manufacturers, academics, government agencies, pharmacy organizations, hospitals and service providers in order to better assess effective tools and strategies to improve REMS effectiveness.
Top Five Reasons to Attend
Stay up to date and understand the FDA’s latest REMS guidelines and standards
Get a thorough assessment of European guidance module 16
Learn how to overcome challenges in a single shared REMS from experienced professionals
Hear case studies on best practices, lessons learned, and successful strategies and tools for REMS design, development and modification by a cross section of small, medium and large companies
Learn how REMS is managed by hospitals and pharmacy organizations
Who Should Attend
Pharmaceutical, biotech and medical device professionals responsible for:
Risk Management/Clinical Risk Management
Drug Safety/Product Safety
Life Cycle Management
Clinical Data Management
Clinical Risk Management Compliance
Medical Writing/Medical Communications
This Event May Also Be of Interest to:
REMS/Drug Safety Service Providers
Data Management Services
Healthcare Regulators and Policymakers
Health Services Research and Academics
Life Cycle Management Services
Group registrations not allowed
Accompanying persons not allowed
We don’t accept Online Abstracts
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