At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings.

Our flagship products, eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process and cleaning lifecycles.  We do not just sell you a software.  Our experienced SMEs will analyze your data and recommend improvements.  

🔍 eResiduePro: 20+ years in use and still the only cleaning lifecycle management software that works.  Designed by Destin LeBlanc, the application captures 30+ years Destin has in this field in its logic.  Be it an API or Formulation or large molecule site, it has the intelligence to understand your site's special requirements and aid you in meeting regulatory requirements.  Simplify your residue calculations and track your cleaning process through validation and ongoing monitoring.

🔄 eProcessPro: A one of a kind solution that tracks every CPP and CQA through the lifecycle, from PPQ runs through OPV runs to APQR generation.  And it has the best data analytics.  

📚 eLogBook: Keep your validation records organized and accessible with eLogBook. Our electronic logbook solution offers a centralized repository for all validation-related documentation, facilitating easy retrieval and audit readiness.

Experience the difference with our innovative solutions tailored to meet your unique requirements.  Reach out to learn more about how Quascenta can support your success!  We can arrange an online demo at a date and time convenient to you.  Contact us at sales@quascenta.com



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