Found 189 results in Expert Content

Summary: Members of our product development gain unparalleled experience working on several products using multiple technologies. Hear what it's like to work​...

Summary: The USP general chapter “Package Integrity Evaluation – Sterile Product” deeply changes the way it considers the Container Closure Integrity Testing (CCIT) within the pharmaceutical...

Lipid formulation and spray-dried dispersions are widely used, and proven technologies to overcome bioavailability challenges for poorly soluble molecules.

Read the latest article published by Pharmaceutical Technology giving an overview of elemental impurities testing and elemental impurities risk assessment process.

This article outlines the preclinical studies to assess and manage developability risks of NMEs for oral drug products

How to create a development strategy that bridges gaps earlier in the process to make the transition smoother.

Lipid-based drug delivery systems provide a reliable solution for poorly soluble molecules

Clarifying the myths surrounding LBDSS which may make drug developers consider it in parallel to other formulation approaches

Developers are looking for ways to predict and overcome potential issues of new molecular entities

Gain more knowledge on dysphagia, which is one of the major factors affecting medication adherence and proper medication administration.