Stability testing on APIs/finished drug product is crucial to ensuring proper packaging for optimum shelf-life storage. Stability testing is essential for maintaining the integrity and quality of ...

As compounds become more multifaceted and biological ingredients are more commonly utilized, stability testing tactics must follow suit and ensure flexibility for developers. WORAWUT - STOCK.ADOBE.COM ...

Stability studies are used to assess the shelf life of a product by storing samples under differing conditions, typically as defined by regulatory authorities, and then testing samples taken from ...

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 ...

This is an intensive two-day masterclass that will help you get a deeper insight into: Analytical Quality by Design (QbD) and Lifecycle Management The Accelerated Stability Assessment Programme (ASAP ...

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 ...

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 ...

Such testing is essential to ensure that the drug product maintains the desired efficacy and purity after transportation and storage. Various constituents of the pharmaceutical product, including the ...

The purpose of the stability testing is to investigate how the raw materials or pharmaceutical preparations will change over time under the influence of temperature, humidity, and light, so as to ...

A three-day residential course organised by the Royal Pharmaceutical Society in partnership with the Academy of Pharmaceutical Sciences. A well-established and up-to-date course designed to provide ...