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
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.
Follow one of these links to discover:
- Additional services offered
- Worldwide use and very high renewal rate
- Our additional lab tools for inventory management
- Our custom development competences
Need further convincing? Choose one or both of the following:
- A real demonstration with one of our statisticians (WebEx conference call)
- A 10 day free trial with a demo version