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    •   Home
        About Us

         Overview
         Customer Support
         FAQs
         Testimonials

    •   Model

        •  As a Service (On-Cloud)

           As a Solution (On-Premise)

        Validation

      Downloads

       Case Studies
       White Papers
       Webinar Videos
       Brochure

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  • Designed by pharmacovigilance experts

  • Cost effective pharmacovigilance solution

  • Compliant with E2B, US FDA 21 CFR part 11 guidelines

  • Integrated MedDRA browser

  • Easy XML file import and export

  • Case validation based on in-built EMA business rules

  • Integrated workflow stages (customizable)

  • Auto narrative generation ensuring consistency across all cases

Sarjen's PvNET in nutshell

  • A single platform for serious adverse event (SAE) reporting for medicinal drugs, medical devices and drug therapies.
  • Global database which fulfills drug safety requirements of multiple regions, viz., Europe, Canada, USA, Australia, etc.
  • Dynamic homepage helps to meet regulatory compliance and maintain work allocation across different users.
  • Add-on functionalities for seamless ADR case processing.

What's New

Veterinary

  • Allows Initial/Follow-up Adverse event reporting of veterinary medicinal products
  • Allows generation of all standard reports like E2B XML, FDA 1932, CVMP
  • Integrated VeDDRA coded terminologies

E2B (R3)

  • New ICH guidelines for electronic submission of Individual Case Safety Report (ICSR) data elements and message specification
  • Sarjen's PvNET integrates these new E2B (R3) guidelines to generate XML's

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