screenshots
Samarind RMS is designed to be an easy to use and intuitive regulatory management package for pharmaceutical professionals.
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View by products
Lists all your generic products, showing the numbers/types of licences approved and pending with all related product details
View by submissions
Lists details of your licence submissions data, providing you with visibility of any critical deadlines and details of all associated manufacturer relationships, etc.
View by licenses
Lists all your generic product licences, showing each licences’ status and providing access to all related documents such as SmPC documentation
View by variations
Lists all your licence variations, showing the current status approved/pending and all associated MA and MRP references
View by companies
Lists all companies relating to your generic products helping you manage key supplier/ distribution accounts and all other key relationships
View by EMEA
Lists and groups all product information in readiness for automated transfer to the
EMEA website via an XML feed and collects a receipt of successful transfer.
Documents
Allows you to manage documents within the system relating to your products and
licences, associated manufacturers and suppliers etc.
View by PSURs
Allows you to automate (as far as possible) the PSUR scheduling process to help
ensure that PSUR’s are submitted in a timely and efficient manner.
Reports
Allows you to produce reports based on various criteria relating to your products and licences, associated manufacturers and suppliers etc.
Admin
Allows you to configure and fine tune the system to best manage all your regulatory affairs
Help
Provides the user with help throughout the entire system
For more details about using Samarind RMS within your business, please contact us.