The United States Pharmacopeia emphasizes mechanical calibration and a performance test to esnure integrity of the dissolution procedure. The intent of the USP performance verification test (PVT), ...

USP applies metrological principles to the dissolution procedure alone and in collaborative studies to understand and minimize potential sources of variability. According to the International ...

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 ...

NEW YORK (PIX11) — The most popularly prescribed drug in the U.S. has been recalled by the Federal Drug Administration. Over 141,000 bottles of Atorvastatin Calcium Tablets, distributed by Ascend ...

Sun Pharma and Wockhardt have separately initiated voluntary recall of a number of drugs from the US market due to different reasons. Sun Pharma initiated voluntary recall of multiple lots of ...

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 ...

SALISBURY, Md.--(BUSINESS WIRE)--Jubilant Cadista Pharmaceuticals Inc. is voluntarily recalling one lot of Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/ 0.02mg, 28x3 Blister Pack/Carton to ...

HYDERABAD:Sun Pharma and Wockhardt Ltd have separately initiated voluntary recall of several drugs from the US market citing various reasons. While Sun recalled multiple lots of Bupropion ...

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 ...