ARS PV

AERs from Post Marketing surveillance & Clinical Trials (CT)

ARS PV

Globally Trusted Pharmacovigilance Database

ARS PV

Global Submission

Submission in different ICH regions with regulatory approved formats.

ARS PV

Compliance

ICH E2B Guidelines,21 CFR Part 11,HIPPA,GxP & GAMP-V validations

An Advanced reporting system for Pharmacovigilance

We wish you to slide into “PROVIDING A SECURE AND BETTER ROAD TO PATIENT SAFETY” by using ARS PV (Pharmacovigilance database) as a gateway to it.

  • ARS PV is an advanced and user-friendly safety database produced and developed by Yuva Infocare Pvt Ltd, An Independent IT organization catering regulatory and business domains. ARS PV is complete solution for Clinical and Post marketing safety surveillance.
  • ARS PV is the pharmacovigilance software system that supports the capture, management, reporting and analysis of adverse events countered from clinical trials and from post marketing surveillance, including cases from literature, of all medical products from drugs to devices, from vaccines to cosmetics.
  • ARS PV core team is always on road to track regulatory developments and rectifications taking place worldwide to keep ARS PV current and updated.
  • For your Pharmacovigilance needs you can confidently rely on ARS PV as your partner for safety technology at current and comings. ARS PV is highly reliable, scalable and cost-effective solution built and designed on latest technological platform, ARS PV is developed on Microsoft .NET Framework 4.5, C# & Entity Framework 6.0. with proved maximum performance, with rapid data processing and user friendliness.
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Some Insights of ARS PV Database

  • ARS PV is globally recognized & fully validated and compliant with EMA, FDA & DCGI regulatory requirements. ARS PV is compliant with FDA 21 CFR Part 11, Annexure 11 and designed as directed in ICH E2B Guidelines. GAMP 5 & HIPPA in Compliance.
  • ARS PV Database facilitates you to perform Quick case processing inbuilt with mandatory field options to create a case, this also enables you to search duplicate existing cases as per the query raised for case creation by AI (Artificial Intelligence).
  • Regulatory Documents i.e Medwatch, CIOMS, E2B XMLs (R2) & (R3) HL7 Import/Export, Line Listing reports are generated in the regulatory approved formats through ARS PV.
  • Inbuilt literature Management tool, ARS PV enables you to perform scientific literature surveillance with user review, case creation and much more.
  • ARS Report builder is an enhanced feature in ARS which facilitates to generate own customized report building with all the available fields selection in ARS Database.
  • ARS database is built with latest technology platform which enables quick process flow and report generation.
  • Assurance on data security and integrity Complete access control system is in place. ARS PV features a highly robust and scalable architecture build leading technological platform and bound to offer you maximum performance, scalability & security promising your data is reliable and secure, no worries you are managing hundreds, thousands or millions of cases.
  • As far as compatibility is concerned it is compatible to run on all available browsers and has compatibility to be used on any screen size.