• 001
    We provide effective and qualitative solutions in the domain of safety of medicines, vaccines and medical devices.
  • 002
    We have the technological tools to capture and analyse reports associated with Adverse Events related to medicines, vaccines and medical devices at institutional, regional and national level.
  • Our Quality management system is ISO 9001:2008 & ISO 27001:2013 certified. We are committed to the robust quality system to ensure the confidentiality and management of information with the highest standards.

Pro Pharma Research Organization

PPROVigi Report
PPROVigi® Report

PPROVigi is a comprehensive application that is useful to anyone who wants to report adverse events (AEs) or suspected adverse drug reactions (ADRs). An AE or suspected ADR is an event or unwanted reaction that occurs after using a drug or vaccine or Medical device, which can be expected or unexpected.

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