Forced degradation studies involve exposing a drug substance to harsher conditions than the product would be expected to experience and determining at what point and how it degrades. Identifying ...

Scientists at Xi’an Jiaotong-Liverpool University (XJTLU) and at Nanjing University have combined a widely used medical polymer with a natural blood protein to develop a new nanoparticle drug delivery ...

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 ...

The data that we collected clearly indicate that the conditions inside the drug compartments of ALS units in Los Angeles County are subject to wide temperature fluctuations, which can become rather ...

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

The Centers for Medicare & Medicaid Services (CMS) standard 42 CFR §482.25(b)(3) states that "Outdated, mislabeled, or otherwise unusable drugs and biologicals must not be available for patient use." ...

Synthetic oligonucleotides are transforming modern therapeutics and advanced analytical strategies are driving confident decision-making to ensure safe and effective development of oligonucleotide ...

Encapsulating drugs within biocompatible polymers allows for controlled release and extended circulation time, optimizing treatment efficacy. These systems also offer tailored formulations, ...