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 ...

MS, and LC-MS/MS testing with ICH Q2(R1)-validated methods, 48-hour turnaround, and pharma-grade documentation for supplements and FBA sellers. IRVINE, CA, UNITED STATES, March 23, 2026 /EINPresswire.

The dissolution profile of inhaled drugs underpins therapeutic efficacy and is an area of increasing regulatory scrutiny, particularly for the demonstration of bioequivalence in a generic. The new ...

Teva is voluntarily recalling a single lot of Anagrelide Capsules, USP 0.5mg, due to dissolution failure that was detected during a routine stability test. Teva is voluntarily recalling a single lot ...