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
Arlenda software is a complete solution for a more streamlined and productive laboratory.
See the benefits:
- Fully validated: Arlenda software is 21 CFR part 11 and GAMP 5 validated.
- Regulatory Friendly: Arlenda software is compliant with global regulatory standards, including: ICH, EP and USP.
- Software-as-a-Service: Access the software via the Internet. All upgrades and maintenance are handled by our administrators and published worldwide.
- Safe Data: Complete encryption, Safely delete all private data from our server data at log-out
- User friendly: Generate your report in less than 10 minutes !
- Focused on decision-making: Extensive use of graphs and charts enhances the decision making process.
WHO USES OUR SOFTWARE
Arlenda Liège Office (Belgium) Avenue du Parc Industriel, 89 4041 Milmort Belgium Phone: +32 10 46 10 10
Arlenda, Inc. (U.S.) 128 Orchard Way, Berwyn, PA 19312 USA Phone: +1 (908) 3462181
RECENT NEWS & EVENTS
December 4-6, 2017 The laboratory landscape continues to face an influx of regulations surrounding the reliability, consistency and accuracy of analytical methods and data. From FDA’s final guidance on analytical procedures to USP chapter updates to FDA and MHRA’s...