pharmaceutical regulatory management
In today’s pharmaceutical industry there are ever increasing demands on regulatory affairs and pharmacovigilance departments; no more so than when managing the submission and maintenance of product licence information to the relevant authorities.
Samarind RMS version 3.0 with full eCTD creation and viewing capabilities...
At Samarind we thoroughly understand these demands and the stringent procedures that can give regulatory professionals a constant headache, such as the enigma of eCTD!
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, including eCTD.
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, as it continues to support leading international pharmaceutical companies with users across the globe. The application is designed to manage the regulatory submissions process end-to-end, including all license submission and variation documentation, automatic uploading of EVMPD data to the EMEA's pharmacovigilance website and eCTD.
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
