Pharmacovigilance

Comprehensive case management

We believe that exceptional pharmacovigilance begins at the individual case report level with high-quality, consistent data capture and management practices. With today’s expanding regulations and growing enforcement, it is more important than ever to utilize proven methodologies and best-practices for managing your adverse event case load.

With Ashfield Pharmacovigilance, you have access to the tools and experience needed to provide a fully compliant drug safety program and a wide array of pharmacovigilance services. From clinical trials safety to post-marketing surveillance, Ashfield Pharmacovigilance manages data collection, triage, tracking, and reporting of your adverse events from start to finish.

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Analyzing, assessing and reporting important safety data requires best practices for data entry, follow-up and query, quality control, medical review and quality assurance. Ashfield Pharmacovigilance adheres to industry-recognized best practices for data management, coupled with thoughtful, business metrics and workflow for enhanced efficiencies.

  • Latest news

    Pharmacovigilance

    03 Oct 2014

    DSA is Ashfield Pharmacovigilance

    Established in the UK in 1997, Ashfield Commercial & Medical Services has eight areas of...

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  • Latest news

    Pharmacovigilance

    01 Jun 2015

    Ashfield attended The World Drug Safety Congress Americas

    The current pharmacovigilance landscape is defined by complex IT systems that require frequent...

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  • Latest news

    Pharmacovigilance

    24 Jun 2015

    Ashfield Pharmacovigilance has a unique advantage in drug safety and pharmacovigilance

    Ashfield Pharmacovigilance has a unique advantage in drug safety and pharmacovigilance due to...

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