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Our Software

Preparing and generating FDA-compliant reports for Method Validation, Method Transfer and Product Stability can be a time-consuming and difficult exercise. 

Arlenda makes it easy. 


E-noval: Validation of your Physico-Chemical methods
Seelva: Validation of your Bioassays
Stab-e-lity: Validation of your products Shelf-life and identification of the Release Limits

Each Software application offers a suite of benefits
  • Fully validated: All arlenda software is 21 CFR part 11 validated.
  • Regulatory Friendly: Arlenda software is compliant with global regulatory standards, including: ICH, GAMP 5, EP and USP.
  • Software-as-a-Service: Access the software via the Internet.  All upgades and maintenance are handled by our administrators and published worldwide.
  • Safe Data: Beside classical security measures, the software automatically deletes all your data from our private server when you log-out
  • User friendly: Simply follow the on-screen steps to generate fully validated reports in 10 minutes or less.
  • Focused on decision-making: Extensive use of graphs and charts enhances the decision making process.
  • SAS-based: All computations are performed using the SAS (Statistical Analysis System) programming language from SAS Institute.
  • 21CFR Part 11 compliant

Considering the above benefits, Arlenda software is a complete solution for a more streamlined and productive laboratory.

See for yourself.  Watch a demo of Arlenda and realize how fast and easy the job is. 

Using the following Arlenda products, you can complete 21 CFR part 11 compliant reports in 10 minutes or less by following 4 easy steps.


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