multiWin pro Advanced TOC/TNb software for regulated environments​

Advanced TOC/TNb software for both routine and regulated environments​

multiWin pro takes TOC/TNb analysis to the next level with a modern, intuitive user interface that simplifies daily operation. Advanced data integrity features support audit‑ready workflows, and optimized algorithms ensure precise, repeatable results. Designed for both routine and highly regulated environments, multiWin pro offers flexible reporting tools, central data management, and easy user onboarding.

Upgrades for users of multi N/C series and multi N/C pharma series instruments

multiWin pro is available as an upgrade for current users of multi N/C series and multi N/C pharma series instruments using multiWin 4 so far. Enjoy all of these modern features easily whilst using your trusted instrument currently working in the lab:

multiWin pro FDA 21 CFR Part 11 Compliance Module

The FDA 21 CFR Part 11 compliance module of multiWin pro is designed to support laboratories in highly regulated environments with a strong focus on data integrity, transparency, and efficiency. It enables secure handling of electronic records and signatures, ensuring full traceability and audit readiness in line with global pharmaceutical requirements. Tailored for modern TOC/TNb applications, the solution seamlessly integrates compliance into daily workflows without compromising usability. This allows laboratories to confidently meet regulatory expectations while maintaining high productivity and reliable analytical performance.

User-Friendly Interface​
The software features an intuitive interface that reduces training time and simplifies complex analytical operations for lab personnel.​

Data Integrity and Audit Readiness​
Advanced data integrity tools ensure audit-ready processes, supporting compliance with regulatory standards in labs.​

Accurate and Reproducible Results​
Highly precise algorithms deliver reliable and reproducible analytical results across various TOC/TNb applications.​

Automation and Central Management​
Supports advanced automation, flexible reporting, and central data management suited for regulated pharmaceutical and industrial labs.​

For more details, feel free to watch our demonstration videos where the functionalities of multiWin pro and the FDA 21 CFR Part 11 Compliance Module are demonstrated: 

multiWin Pro Demonstration Web Seminar

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multiWin Pro Demonstration – FDA 21 CFR part 11 compliance module Web Seminar

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Order Information

Order numberDescription

830-00035-0

multiWin pro  - software upgrade to current version

830-00036-0 FDA 21 CFR Part 11 Compliance module (includes functionalities for central data storage, user management, audit trailing, electronic signatures, and System Suitability Tests)

Downloads

Flyer multi N/C Software (EN)

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Brochure TOC/TN Data Integrity on ALCOA+ Principles

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