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.

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.

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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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  • Latest news

    Pharmacovigilance / Multiple Locations

    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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