記録された日時: March 16 2021
Are you struggling with challenges related to the solubility, stability and manufacturability of your active pharmaceutical ingredients (APIs)?
The Developability Classification System (DCS) provides useful guidelines for selecting an appropriate approach to aid with bioavailability and solubility challenges. However, the guidelines don’t help you address issues related to the stability and manufacturability of pharmaceutical formulations. Overcoming these challenges requires extensive solid-form screening and new formulation types to create competitive pharmaceutical products. Solid form characterization, such as X-ray diffraction, scattering methods and thermal analysis techniques are orthogonal methods that can help you understand the structural and phase behavior of your APIs and excipients. Armed with these techniques you can unlock valuable insights into the properties and stability of a material and their shelf-life profile.
In this webinar we will investigate how the combination of X-ray diffraction, scattering techniques and thermal analysis methods enable thorough characterization.
How these techniques can be used to explain and predict the behavior of an API.
How XRPD, DSC and TGA can aid formulation developers with material selection.
How these techniques can help with understanding the impact of formulation processing operations on product performance.