Hero Banner of Drug Safety and Risk Strategy Exchange, July 30-31, 2024 - American University College, Washington DC

Momentum’s Drug Safety and Risk Strategy Exchange is taking place on July 30-31 at the American University Washington College in Washington, DC.

This time our 4th REMS Innovation Summit and the 3rd PV Oversight & Inspection Readiness Summit will be colocated to potentialize and promote engagement and networking and also for the first time, we are creating the PV & REMS INTERSECTION! 

In this intersection, we will have half a day dedicated to topics of relevance and interest to both the PV and the REMS audiences with interactive sessions and case studies to maximize your time in attendance. Each event has its agenda with thought-provoking sessions and panel discussions while sharing networking opportunities.

Join us on July 30-31 and make sure to invite your PV/REMS peers!

Headshot of Jonathan Banchs
Jonathan Banchs
Senior Director of Content & Experience
MOMENTUM EVENTS

Testimonials

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2024 Speaking

Faculty

2024 SPONSORSHIP OPPORTUNITIES ARE OPEN

Sponsorship is a great way to enhance your brand’s visibility and help you connect with top-level decision-makers, innovators, and industry disruptors. There are a number of ways to maximize branding opportunities at the summit.

Top Reasons to Attend

Grow and foster the relationship between your REMS and your Drug Safety peers to help reduce burdens and secure a more effective oversight and REMS implementation
Discuss effective and compliant REMS and AI applications and explore all the options and possibilities
Participate in active engagement on how to successfully grade your 3rd party vendors
Understand the impact and growth from telehealth and telemedicine and how to accommodate in the REMS space compliantly
Document Safety and Adverse Events Reporting on REMS while being FDA compliant
Grow and foster the relationship between your REMS and your Drug Safety peers to help reduce burdens and secure a more effective oversight and REMS implementation
Examine a practical approach on how Real-world Evidence data should be applied in Drug Safety/PV
Discuss effective and compliant PV AI applications and explore all the options and possibilities
Participate in active engagement on how to successfully grade your 3rd party vendors
Recognize the value of PV systems to streamline communication and achieve inspection readiness

Who should attend?

This event is designed for pharmaceutical, biotech, and medical device professionals with responsibilities in the following areas:

Pharmacovigilance
  • Safety & Risk management
  • Drug safety
  • Technovigilance
  • PV Compliance
  • Safety Surveillance
  • Medical Affairs
  • Regulatory Affairs
  • Inspection and Audit
  • Post-market studies
  • Real-World Evidence Generation
  • Medical product safety assessment
  • Drug Research & Development
  • Clinical Pharmacology
  • Medical information
  • Health outcomes
REMS
  • Benefit/Risk Management
  • Medical Direction
  • Quality Assurance
  • Real-World Evidence Generation
  • Clinical Risk Management
  • Life Cycle Management
  • Regulatory Affairs/Legal/Compliance
  • Clinical Research
  • Clinical Risk Management Compliance
  • Epidemiology/Pharmacoepidemiology