Our supplier Analytik Jena are inviting you to a webinar the 21 of January about TOCnology made for pharma Compliant TOC / TNb-analysis and data handling in regulated environments
LINK: TOCnology made for pharma – Webinar Invitation
Are you analysing TOC or TNb 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 analysers of the multi N/C x300 series from Analytik Jena.
This module and the analysers are the perfect match for customers in the pharmaceutical sector.
They combine convenient operation with data integrity and meet the high demands of compliance while achieving lab efficiency.
New features include, among 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
- Controlled access from any computer
- Detailed audit trail and versioning with comment functions
- Electronic signatures following the dual control principle
In the webinar our experts will talk about:
- 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 the new software module offers
- The new FDA 21 CFR Part 11 software module of the multi N/C x300 series
- 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