Perform Conductivity Measurements in Compliance with USP <645>
Learn more about USP <645> requirements, along with tips and tricks on how to meet specifications
USP Compliance
Preparation of Pharmaceutical Samples in Accordance with USP <232>/<233>
Utilizing single reaction chamber (SRC) sample prep technology for trace metals analysis of pharmaceutical samples
Analytical Method Validation: Do It Now or Pay Later
Thorough method validation can be tedious, but not doing it right means wasted time, money, and resources
Complying with the New USP General Chapter on Analytical Instrument Qualification
This live webinar event will review requirements for the new USP General Chapter on Analytical Instrument Qualifications (AIQ)
How Transferring Validated HPLC Methods Within USP Guidelines Works
Problem: The topic of technology transfer raises caution with many laboratory managers of analytical laboratories. In routine analysis laboratories, such as QA/QC, the need for continued support of established high performance liquid chromatography (HPLC) methods can significantly outweigh the potential advantages of method modernization, making it exceptionally problematic or undesirable to adopt more modern liquid chromatography (LC) assays or instrumentation such as U(H)PLC ultra-high performance LC.
METTLER TOLEDO’s Weighing Standard Ensures USP Compliance
On the 3rd June, 2013, United States Pharmacopeia (USP) published the revised mandatory Chapter 41 on balances as well as new updates to the advisory Chapter 1251. With just six months to comply, METTLER TOLEDO’s global weighing standard, GWP®, can help pharmaceutical manufacturers and suppliers to meet the new requirements.