Industry, equipment vendors, and regulators are busy refining the precision and reliability of dissolution testing. Solid dosage formulators rely on dissolution testing to mechanically model the ...

Industry experts discuss best practices for dissolution testing of poorly soluble, immediate-release, and controlled-release formulations and the different analytical approaches used. Dissolution ...

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 ...

Dissolution testing plays an important role throughout the life cycle of a pharmaceutical product, i.e., from evaluating how quickly a compound dissolves into solution in controlled conditions to ...

SARASOTA, FL, Oct. 31, 2024 (GLOBE NEWSWIRE) -- Silo Pharma, Inc. (SILO) (“Silo” or the “Company”), a developmental stage biopharmaceutical company focused on developing novel formulations and drug ...

Do you work in formulation development or the testing of tablets? Do you require an intensive course of study on the relevance, development, validation and routine use of dissolution testing? This new ...

The global Pharmaceutical Dissolution Testing Services Market is anticipated to reach US$ 693.12 Million in 2023 and US$ 1,538.48 Million by 2033, with a CAGR of 8.3% from 2023 to 2033. The expansion ...

Distek, Inc., a leading manufacturer of laboratory testing instruments for the pharmaceutical and biotechnology industry, as well as an experienced provider of validation and qualification services, ...

Dublin, Oct. 29, 2025 (GLOBE NEWSWIRE) -- The "Pharmaceutical Dissolution Market - A Global and Regional Analysis: Focus on Type, End User, and Region - Analysis and Forecast, 2024-2033" has been ...

The implant demonstrates stability and consistent drug release, supporting further analytical testing and development SARASOTA, FL, Oct. 31, 2024 (GLOBE NEWSWIRE) -- Silo Pharma, Inc. (Nasdaq: SILO) ( ...