Key market opportunities in dissolution testing include optimizing drug bioavailability and enhancing quality control to meet regulatory demands. Understanding scientific principles and regulatory ...
In the manufacture of solid dosage forms, the rate at which the active pharmaceutical ingredient (API) is dissolved into solvents simulating the digestive tract fluids is determined with dissolution ...
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 ...
The Media-Mate Plus is the perfect media-prep system for a busy dissolution lab that demands both speed and accuracy. It delivers pre-heated, filtered, deaerated, and volumetrically dispensed media to ...
(NEXSTAR) – Over 141,000 bottles of cholesterol medication have been recalled due to “failed dissolution specifications,” suggesting that the drugs did not pass a solubility test, or failed to ...
Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary ...
A popular ADHD medication is facing a nationwide recall because tests suggest users will not benefit from the full effect of ...
The most popularly prescribed drug in the U.S. has been recalled by the Federal Drug Administration. Over 141,000 bottles of ...
Jubilant Cadista has issued a voluntary recall of one lot of birth control pills produced under contract by Cyndea Pharma in Spain because it failed dissolution tests. The recall covers blister packs ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback