Pharmaceutical testing is a must to ensure that all medications meet the top quality, safety, and performance requirements before they enter the market. CD Formulation’s cGMP-compliant laboratory is ...

The disintegration time of the RDT in water was determined using the apparatus of the Japanese Pharmacopoeia (JP) 14 disintegration test, without a disk for six tablets. The 1000 mL of deionized and ...

The authors describe the various available technologies used in orally disintegrating tablets. This article is part of PharmTech's supplement "API Synthesis and Formulation 2009." New drug-delivery ...

CD Formulation owns a cGMP-compliant laboratory and a team of experts. Together with state-of-the-art analytical instruments, the company is capable of conducting analytical process development and ...

Dublin, Feb. 06, 2024 (GLOBE NEWSWIRE) -- The "Orally Disintegrating Tablet Market - Global Industry Analysis, Size, Share, Growth, Trends, and Forecast 2031 - By Product, Technology, Grade, ...

Rockville, MD, Oct. 16, 2024 (GLOBE NEWSWIRE) -- Based on a new research report published by Fact.MR, the global orally disintegrating tablet market is poised to reach a valuation of US$ 24.45 billion ...