The Evolving Pharmacovigilance (PV) Landscape
Viewpoint

30 Sep 2022
by Ankur Verma, Gokul Janardhan

The rising burden of chronic diseases worldwide is driving life sciences companies’ drug development efforts. These drug development efforts need to abide by the strict drug safety regulations of public health organizations, such as the US Federal Drug Administration (FDA) and the European Medicines Agency (EMA). The regulatory protocols mandate the prior- and post-marketing safety assessment of drugs and are increasingly pressing biopharma and medical device companies to effectively capture, assess, and monitor Adverse Events (AEs) to gain the trust of both regulators and consumers.

In this viewpoint, we focus on the challenges that face the US$19 billion Pharmacovigilance (PV) market amid increasing AEs and changing regulations. We also look at the measures that life sciences enterprises have adopted in tackling these challenges, including partnering with third-party providers for technology solutions.

Industry

Life Sciences BPS

Geography

Global

Contents

This report provides a detailed analysis of the PV landscape, including:

  • Emerging challenges for life sciences enterprises
  • Enterprise adoption of point solutions
  • The role of third-party providers
  • Current state of the PV market

Membership (s)

Life Sciences Business Process

Sourcing and Vendor Management

 

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