Article | July 10, 2020

Global Pharmacovigilance Readiness Checklist

Source: United BioSource LLC (UBC)

Having a comprehensive understanding of your organization’s readiness to tackle any or all safety responsibilities is paramount.

The right strategy to continually evaluate product safety in your clinical trials, through regulatory review and entering the post-marketing setting, is complex. Local market regulations are ever-changing. Technologies to intake, track and manage workflow are getting more sophisticated. Expectations of global regulators are increasing regarding ongoing, long-term safety assessments, signal detection and refinement. Are you ready?

UBC has assembled this “PV readiness” checklist to enable our clients to drive internal conversations around their safety strategies, and ensure they have a partner in place to help in any or all of these important categories of a safety organization.

VIEW THE ARTICLE!
Signing up provides unlimited access to:
Signing up provides unlimited access to:
  • Trend and Leadership Articles
  • Case Studies
  • Extensive Product Database
  • Premium Content
HELLO. PLEASE LOG IN. X

Not yet a member of Clinical Leader? Register today.

ACCOUNT SIGN UP X
Please fill in your account details
Login Information
ACCOUNT SIGN UP

Subscriptions

Sign up for the newsletter that brings you the industry's latest news, technologies, trends and products.

You might also want to: