Live Webinar: Pharmacopoeial Changes, Are Your Weighing Processes Ready?
Stay Compliant with the Latest USP <41> and Ph. Eur. 2.1.7 Requirements
Panoramica del programma
- Impact of the latest USP and Ph. Eur. 2.1.7 revisions
- Understanding the new safety factor concept
- Measurement uncertainty requirements and their practical implications
- The significance of as-found and as-left results
- Considerations for multiple range and multi-interval balances
- How to select balances that support compliant weighing
- Calibration and qualification services that help maintain compliance
- Live Q&A session with our experts
Recent updates to USP <41> and Ph. Eur. 2.1.7 introduce significant changes to the way pharmaceutical laboratories demonstrate weighing performance. New concepts such as the safety factor, measurement uncertainty requirements, and as-found/as-left calibration will influence both qualification strategies and routine weighing activities.
In this webinar, our weighing experts will explain the practical implications of these changes for pharmaceutical quality control laboratories. You will gain insight into selecting suitable balances, understanding compliance expectations, and leveraging calibration and qualification services to support audit readiness.
Who Should Attend?
This webinar is particularly relevant for: Pharmaceutical Quality Control professionals, Quality Assurance specialists, Laboratory Managers, Validation and Compliance professionals, Metrology and Calibration specialists, Professionals responsible for laboratory audit readiness
Speakers
Dr. Klaus Fritsch
Manager Compliance at Laboratory Weighing, METTLER TOLEDO
As senior metrologist and regulatory expert, Klaus consults the industry to achieve compliance with regulations when using weighing instruments. Klaus is expert advisor for USP and Ph. Eur. and contributing author to calibration guidelines of EURAMET and ASTM.
