Show Overview

We look forward to seeing you February 27-28, 2023!

Drug Safety Summit Description Image

Furthering Drug Safety Operations Through Industry Education

The Fierce Drug Safety Summit brings thought leaders from across pharma, biotech, and device companies to explore current challenges faced when ensuring the safety of patients. Leaders in pharmacovigilance, drug safety, risk management, and regulatory affairs will discuss the most effective ways to institute a risk management program and be better equipped to meet government regulations.

Optimize your Drug Safety Operations by Attending Sessions from our Two Tracks

Risk Management & REMS

FDA Updates
Risk Management Plan Development
Vendor Engagement
Regional Differences


Global PV
FDA Guidance
Technological Advancements
Inspection Readiness

Why You Should Attend

Regulatory Updates
Regulatory Updates
Hear updates from the FDA on new guidances passed
Learn How to Plan
Learn How to Plan
Understand how to develop a global risk management plan ensuring compliance across regions
Stay Ahead of Current Trends
Stay Ahead of Current Trends
Learn how to navigate the current changing landscape of REMS management
Technology Updates
Technology Updates
Learn how to properly incorporate AI and machine learning technology into PV operations to enhance practices and cut costs
Networking Opportunities
Networking Opportunities
Connect with Heads of REMS and PV operations to gain insights and best practices on daily challenges faced within these fields
Hear from Susan Welsh, MD, Senior VP, Pharmacovigilance and Chief Safety Officer at Mirati Therapeutics on Why this is a Must-Attend Event for Drug Safety Professionals

 Who Should Attend

This conference is designed for representatives from pharma, biotech, and medical device companies with responsibilities in the following areas:

  • REMS
  • Risk Management
  • Pharmacovigilance/Surveillance
  • Quality Assurance
  • Drug/Product Safety
  • Clinical Risk Management
  • Lifecycle Management
  • Regulatory Affairs/Legal/Compliance
  • Clinical Affairs
  • Clinical Data Management
  • Clinical Operations
  • Clinical Risk Management Compliance
  • Epidemiology/Pharmacoepidemiology
  • QPV
  • PV Technology
  • Clinical Trials
  • Patient Access
  • Global PV
  • Patient Safety
  • Adverse Events/ Reporting

Attendance by Seniority Level

We bring together leaders in REMS and Pharmacovigilance... Over 57% of our previous attendees are director-level and above!