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Lorenz Products Portfolio

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

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Collect and manage all product data in a single place:
- Prepare your data for IDMP
- Submit medicinal product data (xEVMPD)

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Manage changes throughout the entire product life cycle

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Automate the standardized processes in your workflow

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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?

Click here

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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

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