Building on the reliability of the industry-leading Agilent 8000 autosampler, the 850-DS provides even more capabilities for pharmaceutical QA/QC customers. The 850 ...
Missed or late calibration dates can accumulate, and even if the equipment is labelled appropriately, it can suggest poor management of resources and priorities. Good manufacturing practice (GMP) ...
Despite its importance in drug development, dissolution testing still has some limitations, but advances in automation and real-time monitoring are producing promising results. The importance and ...
DUBLIN--(BUSINESS WIRE)--The "Troubleshooting Dissolution Methods for Solid Oral Dosage Forms" webinar has been added to ResearchAndMarkets.com's offering. By attending this webinar, you will learn ...
Dissolution and drug release tests are directly relevant to the safety and efficacy of many common pharmaceutical dosage forms. To achieve reliable and reproducible results, analysts must understand ...
Pharmaceutical dissolution testing for solid oral dosage forms is a complex analytical procedure where the control of critical variables (environmental conditions, equipment performance, sample ...
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