TOC/TN Cleaning Validation

How to approach pharmaceutical cleaning validation by sum parameters – challenges and solutions

This web seminar focuses on overcoming key challenges in TOC/TN cleaning validation for the pharmaceutical industry.
Topics include method sensitivity, complete oxidation verification, compliance with international standards, calibration strategies in the trace range, and contamination risks for samples and QC standards. We’ll also cover establishing reliable recovery rates for swab and last rinse techniques. Additionally, learn about essential software features for compliance—secure data storage, user authentication, audit trails, electronic signatures, and role-based management. Finally, discover Analytik Jena’s solutions with the multi N/C x300 series, including equipment qualification, software validation, and upgrade services.

Duration: ~60 min
Language: English
Speakers:
Bernd Bletzinger, Product Manager TOC
Ann-Sophie Lehnert, Product Manager Software & IoT

Key Topics:
- Methods of cleaning validations
- Key challenges including method sensitivity, proof of complete sample oxidation, calibration strategies in the trace range, contamination risks for samples and QC/calibration standards.
- Meeting pharmaceutical compliance standards

Learn more: Visit our website for full details on the web seminar.