Compile, publish, import and review submissions such as:
- eCTD
- (V)NeeS
- PDF
- and other formats for many regions
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Manage content of an application/sequence which requires:
- a lifecycle and versioning
- permission rights
- editing/viewing restrictions
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Validate submissions such as:
- eCTD
- (V)NeeS
- PDF
- and other formats for many regions
|
Collect and manage all product data in a single place:
- Prepare your data for IDMP
- Submit medicinal product data (xEVMPD)
|
Manage changes throughout the entire product life cycle
|
Need more than one of our business capabilities? Combine our solutions to create your own flexible Regulatory Information Management system (RIMS).
Learn more…
Do you want to get a first look at how our RIM solution can provide you with a seamless experience?
Icon Explanation
Single user
small- to mid-sized company
Mid- to large-sized company
Regulatory agency
Deployment in the cloud
Deployment on a local server
Deployment on a local workstation