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Preparing Your Drug for Clinical Success: Strategies and Considerations

Summary:​ The pharmaceutical industry continues to experience decreasing productivity and high levels of attrition. Inflation of molecule physicochemical properties and complexities in clinical trial protocols stand among the main reasons for these trends. The most successful companies can leverage different expertise, manage risks, and follow logical sequences of operations in an integrated manner to speed development.

This webinar focuses on the key considerations for transitioning a molecule from discovery through clinical studies including molecule developability assessment, phase-appropriate formulation selection, integration of product development and clinical supply, as well as regulatory requirements for advancing a developmental candidate to clinical trials.

Click here to watch the webinar