key features
Key features of Samarind RMS include:
- Event tracking for drug licensing applications and renewals
- Time stamped historical audit of all previous submissions and variations
- System generated notifications by email at key stages
- All data and documents contained within a single SQL database for security, robustness and performance
- Fully networked for multi-user and remote use
- A modern, user friendly graphical interface.
To ensure Samarind RMS remains in line with the regulatory process, we are continuously developing the application, introducing new feature sets, such as document creation and version control and PSUR scheduling. We are currently working on providing additional features and tools to help with eCTD submissions.
As a Samarind RMS user you will receive all generic updates as part of your annual support contract, and we actively seek your input regarding what new features the product could include. Alternatively, if you have any company-specific requirements, with our vast experience of developing bespoke business software, we can of course customise Samarind RMS to precisely meet your exact needs.
For more details about using Samarind RMS within your business, please contact us.
