QbD1200 Laboratory TOC Analyzer

Temporarily not available for purchase.

For your TOC analysis needs, please consider the ANATEL PAT700. Click here for more information.

The new QbD1200 TOC analyzer is designed to make testing easier, reproducible and accurate. The new TOC analyzer promises highest performance while dramatically reducing cost of ownership by using one reagent for the test and requiring only one annual service call rather than frequent maintenance. The new TOC analyzer eliminates the dependency on lengthy overnight routines that may fail. In the first of its kind the QbD1200 TOC analyzer calibrates in only 90 minutes. The QbD1200 is designed for use in 21 CFR part 11 lab environments and is fully compliant with all global pharmacopeia regulations. It offers convenient validation as it is not operated by a separate PC eliminating the need for an additional CSV file and provides paperless reporting to distribute all auditable reports over secure protocol to a central server.

Documentation and Application Notes

Resources + Tools
21 CFR Part 11 FAQs Request Quote Tech Docs
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QbD1200 TOC Analyzer Features

Reliable data

Stop throwing away your first sample! The QbD1200+ has virtually eliminated sample-to-sample carryover! Highly repeatable results!

Simplify your validation and analysis

Automated calibrations, System Suitability Testing and report generation! Only one reagent is needed for ALL analysis!

Low cost of ownership & fast calibration

Say goodbye to frequent maintenance, and reduce your service calls. Automated calibration in less than 90 minutes saves the user precious time and is the fastest in the industry!

Ensure regulatory compliance

Fully complies with all global pharmacopeia regulations: USP, JP, EP, IP, ICH.

Introduction to the QbD1200 TOC Analyzer

 

Content and Resources

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QbD1200 Evaluating Carryover Technical Note
Achieving Compliant Batch Release – Sterile Parenteral Quality Control This paper describes common QC instrumentation compliance elements and gives examples of best practice for instruments used for compliant QC batch release.
Detection Limit For Detection Limit (DL), often referred to as Limit of Detection (LOD), both ICH and JP 16 offer clear direction.
ICH Q2 – the Challenge of Measuring Total Organic Carbon in Modern Pharmaceutical Water Systems <span style="color: #4d4d4d;">Total Organic Carbon (TOC) is one of the quality attributes defined in the European and USA pharmacopoeias for pharmaceutical waters</span><span style="color: #4d4d4d;">. Modern water treatment systems can deliver such high purity water that TOC levels can be consistently close to zero and very difficult to measure with any accuracy. This paper discusses some of the challenges when using TOC analysers to demonstrate pharmacopoeial TOC level compliance for modern water systems in the light of the ICH Q2 document</span><span style="color: #4d4d4d;">2</span><span style="color: #4d4d4d;">&nbsp;from the International Conference on Harmonisation.</span>
Calibrating the QbD1200 TOC Analyzer The calibration of a TOC Analyzer is a crucial part of ensuring a quality measurement.

Technical Documents

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