Improve pharmacovigilance responses and drug risk–benefit analyses with efficient, accurate, comprehensive and compliant adverse event capture, assessment and reporting.

Leverage our dedicated R&D Solutions for PV to:

  • Generate information search strategies that have high recall and precision
  • Quickly detect adverse event information across various types of scientific literature
  • Easily search FDA/EMA drug approval and comparative drug safety data and FAERS reports
  • Automate and centralize information management with a GxP-compliant pharmacovigilance workflow management tool
  • Quickly generate audit-ready reports
  • Track progress and manage the workload of literature review staff members

Webinar thumb - Enhancing key PV Solutions | Elsevier

Enhancing key PV Solutions to boost the efficiency of drug safety workflows

See our exclusive webinar focusing on our 2018 enhancements to Embase, PharmaPendium and QUOSA PV. Discover what’s changed and how it improves the monitoring of relevant databases, assessment of captured information, and supervision of the workflow.

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Elsevier's R&D Solutions for Pharmacovigilance

Thousands of pharmacovigilance and drug safety teams at pharmaceutical companies rely on Elsevier’s R&D Solutions and services. We have focused on providing comprehensive coverage of drug safety data sources and alleviating challenges with pharmacovigilance processes.

QUOSA

Promote efficiency and organizational compliance. QUOSA centralizes the discovery of adverse event information from multiple sources and automates information monitoring and triage in a scalable, GxP-compliant environment.

Discover QUOSA

PharmaPendium

Make more informed decisions on drug safety and efficacy, risk, and study design. PharmaPendium delivers comparative drug interaction data and facilitates searches of FDA and EMA drug approval document sources, including FAERS.

Discover PharmaPendium

Embase

Improve monitoring of biomedical literature for adverse events. Embase is the world’s most comprehensive database of peer-reviewed and grey biomedical literature. It includes crucial non-English content and offers unique support for search design.

Discover Embase

Professional Services

Let informatics and analytics experts support your drug safety goals. Our Professional Services team can streamline adverse event and safety signal detection by validating search strategies and implementing solutions for literature triage and review.

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White Paper - Embase | Elsevier

What is the key to more efficient risk–benefit analysis?

A strong drug safety strategy with efficient risk–benefit analysis is a commitment to patient safety and a healthy drug life cycle. This new white paper assesses the five steps to follow in building an efficient, accurate and compliant strategy for capturing and reviewing adverse event information from the biomedical literature.

See the white paper

Best practices for building PV search strategies

This new application note gives a step-by-step example of building a search for adverse drug events using Embase’s PV Wizard. The method described can be applied to any pharmacovigilance-focused search of the biomedical literature.

Read the application note

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thumbnail-of-quosa-factsheet | Elsevier

How QUOSA works

See how our workflow management tool promotes efficient and compliant pharmacovigilance. QUOSA helps you automate monitoring of relevant databases, streamline assessment of captured information, and more easily supervise the workflow.

Download the fact sheet (PDF, 359.2 KB)


Customer story

Ensuring compliant monitoring of adverse events

Compliance is critical in the highly regulated world of pharmacovigilance. Find out how Elsevier’s Professional Services team helped one pharmaceutical company improve the compliance of their literature screening.

See the case study

Ensuring compliant Monitoring of Adverse Events - Professional Services | Elsevier


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