Found 463 results in Expert Content

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

We will review the current OTC remedies for cough, cold and allergy categories and discuss strategies to grow your share on shelf space with innovative dosage forms.

Watch this webinar to learn the key considerations for evaluating available technologies to find the most suitable bioavailability solution.

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.