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) ...
Industry experts examine the fundamentals of dissolution testing, including challenges resulting from an increasing number of poorly soluble molecules under development in the pharmaceutical pipeline.
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 ...
To achieve reliable and reproducible results, it is important that analysts understand the importance of correctly setting up and sampling from the chosen apparatus. In addition to use of dissolution ...
Pharmaceutical dissolution testing for solid oral dosage forms is a complex analytical procedure where the control of critical variables (environmental conditions, equipment performance, sample ...
To achieve reliable and reproducible results, it is important that analysts understand the importance of correctly setting up and sampling from the chosen apparatus. In addition to use of dissolution ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results
Feedback