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Web Seminar: TOCnology made for pharma

Tuesday, January 21, 2025 | 9 AM and 4 PM CET

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Web Seminar: TOCnology made for pharma Efficient and compliant TOC / TN-analysis and data integrity in regulated environments

Contents of this web seminar

When: January 21, 2025 | 9 AM and 4 PM CET (12 AM and 7 AM PST)
Duration: ~60 min
Language: English
Speakers:
Bernd Bletzinger, Product Manager, Analytik Jena
Ann-Sophie Lehnert, Product Manager, Analytik Jena

Are you analyzing TOC or TN in the highly regulated pharmaceutical sector? Then you should get to know the new FDA 21 CFR Part 11 software module for the new TOC/TNb analyzers of the multi N/C x300 series from Analytik Jena releases. 

This module and the analyzers are the perfect match for customers in the pharmaceutical sector: they combine convenient operation with data integrity and to meet the high demands of compliance while achieving lab efficiency. New features include, amongst others, a user management system for assigning roles and editing rights to team members, server-based central data management to store data from multiple instruments and access them from any computer, detailed audit trail and versioning with comment functions, and electronic signatures following the dual control principle. 

Our experts will discuss with you:

  • which device of the multi N/C x300 series is best suited for your pharma application
  • what challenges the pharma regulations have for TOC / TN analysis
  • what features of the new software module offers 

Get to know the new FDA 21 CFR Part 11 software module of the multi N/C x300 series in our launch web seminar, and learn how to benefit from significant time saving and operating comfort when performing audit-proof analyses in this strictly regulated industry. 

Who Should Attend:

  • Lab managers in pharmaceutical labs
  • Quality assurance officers in pharmaceutical labs
  • Quality control experts in pharmaceutical labs

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