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Read this article published by Pharmaceutical technology to learn about proven strategies for a successful product launch, including cross-functional team collaboration, risk management and using the right project management tools.

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

Understand why new therapies fail or succeed in the market place and learn when and how to apply advanced technologies to help increase the chance of success

Elemental impurities can arise from a variety of sources, such as active pharmaceutical ingredients (API), excipients, manufacturing equipment, and primary container closure systems.

Strategies companies can use to succeed in both advancing their candidates and attracting investors

Solid form screening and selection is an integral part of drug development.

Quality by Design (QbD) is well established in the pharmaceutical industry for manufacturing processes, including active pharmaceutical ingredients and drug products.

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

Roller compaction is a popular dry granulation process with some significant advantages over wet granulation processes.

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