GMP release and stability testing are indispensable elements of the pharmaceutical sector’s quality assurance strategy. These testing protocols not only ensure that pharmaceutical products are safe ...

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 ...

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 ...

Intertek the leading quality solutions provider to industries worldwide today opened a new 8000 ft² 190000 litre pharmaceutical stability storage facility in Royston UK in response to increased client ...

Pharmaceutical companies follow strict quality standards, and if a drug’s stability falters at any point – whether during development, storage, or shipping, it can undo all the work that’s gone into ...

New and important techniques in stability testing are facilitating product development using the Quality by Design approach. Using these it is possible to develop products more quickly and reliably, ...

The use of acidic MPAs (pH 2–4) is the default in pharmaceutical testing because they suppress silanol ionization (from Si-OH to Si-O -) and improve peak shape for basic drugs. However, highly ...

DUBLIN--(BUSINESS WIRE)--The "Pharmaceutical Analytical Testing Outsourcing Market Size, Share & Trends Analysis Report by Service (Bioanalytical, Stability, Method Development & Validation), by ...

While still trying to address an FDA warning letter issued nearly two years ago, New Jersey pharma Teligent says it’s yanking a lot of its topical pain numbing treatment after testing found the med to ...