From Molecule to Medicine: Understanding the Challenges and Solutions in Solid Dose Development

The development of a pharmaceutical product can be a difficult journey to navigate with lots of ups and downs along the way. Many challenges can arise that pose a risk to timelines, cost and even clinical success.

In this seminar you will learn:

• The importance of characterization and understanding API properties, and how these can affect the drug substance and drug product manufacturing process

• Recommended approaches in early phase development to achieve speed to clinic with a suitably robust product

• How to balance the amount of effort invested early on, in order to prevent financial risks and delays from occurring in late stage development

• The scientific solutions and expertise to scale oral solid dosage forms from API to packaged finished product