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multiWin Pro Demonstration FDA 21 CFR part 11 compliance module

Content and goals of the Web Seminar

Duration: ~10 min
Language: English
Speakers:
Ann-Sophie Lehnert, Manager Software & IoT, Analytik Jena
Bernd Bletzinger, Product Manager TOC, Analytik Jena

For TOC/TN applications in the pharmaceutical environment, an FDA 21 CFR Part 11 Compliance module is available for multiWin pro. Curious how it makes your TOC/TN analysis in the pharmaceutical environment compliant and efficient? Our demo video reveals how the compliance module in multiWin pro makes data handling easy and efficient with:

  • Audit-safe, centralized data handling of all of your multi N/C x300 devices
  • A detailed user management with user roles
  • Signatures for a clean release process
  • Integrated SSTs (System Suitability Tests)

Designed for the multi N/C x300 series, this module brings powerful compliance features to your fingertips—and upgrade options are available for other multi N/C analyzers too.

Watch the demo and discover how compliance can be this simple.

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