ISO 9001:2015 and the implications on weighing devices
Managing risk and quality in compliance with the latest ISO revision
This white paper explains the changes in the revised standard of ISO 9001:2015 and describe the timeline associated with transition to the new version.
No Weighing with a Blocked Balance
All balances undergo a monthly repeatability test in accordance with U.S. Pharmacopeia
Micro-weighing guide: 10 steps to successful micro-weighing
Learn how to maximize the quality of your weighing results and make the delicate process of micro-weighing more efficient
To make the most of your smallest quantities and ensure user safety, check out the tips and tricks in our guide "10 Steps to Successful Micro-Weighing"
Secure Traceability in Balance Testing with Verified Weight Identification
The security and compliance of balance testing can be assured by using WeightLink™. This innovative approach makes it possible to use validated test
Daily Sensitivity Test
Check the Sensitivity of Your Balances
As is the case for a number of other businesses, the pharmaceutical industry tends to have strictly regulated areas, for example in quality control procedures
How to Reduce Uncertainty in Weighing?
Accurate Results with Standard Operating Procedures for Periodic Eccentricity Tests
In weighing accuracy is everything. Every little thing matters.
Quality Improvements in Weighing Via Process Tolerance and Safety Factor
When weighing is used in production, significant quality improvements are made possible by managing weighing process tolerances.
What is the Correct Way to Check Repeatability in Balances?
Consistent Outcome Every Time with Standard Operating Procedures for Periodic Repeatability Tests
Your balance must provide the same result for repeated weighing of the same load under the same measurement conditions.
Gravimetric sample preparation – reducing sample size and OOS errors
The benefits of gravimetric sample preparation compared to traditional volumetric methods
Over 50% of out-of-specification (OOS) results in analytical workflows are reportedly caused by sample processing and operator errors
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