Table III. Pharmacokinetic parameters for rebamipide following oral administration of granules or a tablet at a dose of 100mg in 27 healthy adult male volunteers [mean (SD)] ...

New Delhi: Exemed Pharmaceutical has got approval from the Subject Expert Committee (SEC) functional under the Central Drug ...

Novotech, the leading global full-service clinical Contract Research Organization (CRO), has ...

The Income Tax Department has searched the offices and manufacturing units of a contract development and manufacturing ...

Nat Clin Pract Endocrinol Metab. 2006;2(9):474-475. J.V. Hennessey is an Associate Professor of Medicine at the Brown Medical School, Rhode Island Hospital, Providence, RI, USA. Disclosure: The ...

TAHO Pharmaceuticals is pleased to announce the successful completion of the pivotal trial for TAH3311, the first anticoagulant oral dissolving film (ODF). This trial was conducted following detailed ...

The Internship Program 2024 for medical students and graduates was successfully concluded at the Dr. Panjwani Center for ...

The new single-injection dosage was approved on Oct. 14, 2024, based on studies that evaluated the bioequivalence of the drug’s 320 mg dose given as a 2 mL subcutaneous injection vs. two 1 mL ...

An Abbreviated New Drug Application (ANDA) is an application submitted to the U.S. FDA to demonstrate that a generic drug is equivalent to a previously approved Reference Listed Drug (RLD) in terms of ...

Min Son of Hanol IP & Law says pharmaceutical R&D in South Korea should be enhanced on the introduction of a clearer legal framework that offers improved market protection for new and modified drugs ...

In 2024, the Hatch-Waxman Act continued to play a critical role in the U.S. pharmaceutical landscape, driving the dynamics between ...