From raw material identification to finished and packaged pharmaceutical products, stability testing is a critical step for both research and development (R&D) and quality control (QC), with a ...

Biologics stability testing in pharmaceutical R&D typically requires weeks of waiting between processes. Formulation scientists must develop, assess, and then wait to discover if a formulation remains ...

Turbiscan technology accelerates lipid nanoparticle stability testing and supports robust pharmaceutical formulation ...

Stability testing is essential in the pharmaceutical and biopharmaceutical industries. These tests are performed to evaluate the stability of drug products under various environmental conditions. Once ...

Before taking our survey, 16% of respondents were not aware of the CMS regulation and interpretive guidelines that require pharmacists to store drugs and biologicals in accordance with the ...

Safety and efficacy are the two regulatory benchmarks for pharmaceutical products. Microbial contamination of products is an important aspect of product quality that can affect both safety and ...

As a central pillar of modern society, the pharmaceutical industry bears the load of billions of lives around the world. In 2022, the global revenue of the pharmaceutical industry approximated $1.5 ...

Data integrity, impurity characterization, and stability requirements are key focus areas in drug substance testing, with advanced analytical technologies enhancing accuracy. Newer modalities, ...