pharmaceutical regulatory management

In today’s pharmaceutical industry there are ever increasing demands on regulatory and pharmacovigilance departments; no more so than when managing the submission and maintenance of product licence information to the relevant authorities.

Samarind RMSSamarind RMS is currently supporting regulatory professionals in 28 countries...

At Samarind we thoroughly understand these demands and the stringent procedures that can give regulatory professionals a constant headache. Working closely with experienced pharmaceutical industry professionals, we have developed Samarind RMS, a robust user-friendly software application which precisely manages the key areas of product licence acquisition and maintenance.

Like all of Samarind's tried and tested applications, our Samarind RMS software for the pharmaceutical industry is earning a strong reputation for delivering results time after time. Already proven with a number of international pharmaceutical companies the application is designed to manage the submissions process end-to-end, including all license submission and variation documentation and the automatic uploading of EVMPD data to the EMEA's pharmacovigilance website.

Key benefits of Samarind RMS

  • reduces the costs of managing your licences
  • improves accuracy of regulatory data
  • provides fast and accurate reporting
  • provides greater flexibility of working
  • improves overall efficiency of regulatory data management
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