WebIn order to obtain the solid-state form with desired properties, solid state screening needs to be performed. Polymorph, co-crystal, salt screening, amorphous solid dispersion are most common solid state screening methods of which, polymorph screening is still most widely applied. You can accelerate your crystallization research with the ... WebOur solid form screening work programs can be seamlessly progressed into crystallization process development studies, scaling the nominated solid form from milligram to multigram scale in preparation for further manufacturing. Crystallization process development
Polymorphs, Solvatomorphs, Hydrate, and Perhydrate of …
WebMar 8, 2024 · Our screening technology is to design various crystallization conditions according to the physicochemical properties of the target compound and factors affecting drug crystallization, to screen and … WebThe shelf-life, bioavailability and processability of an active pharmaceutical ingredient depends on the crystal form and screening for new solid-state forms including polymorphs, salts and cocrystals is now a routine part of the drug development process. A range of techniques are used to obtain different solid-state forms with high phase purity. cmcas angouleme
SOLID FORM SCREENING - Phase Appropriate …
WebOur screening technology is to design various crystallization conditions according to the physicochemical properties of the target compound and factors affecting drug crystallization, to screen and discover the most … http://cepac.cheme.cmu.edu/pasi2008/slides/doherty/library/reading/Doherty_From_Form_to_Function_AIChEJ2008.pdf WebFeb 23, 2024 · Crystal16 as a multi-functional tool for solubility, solid-form screening, and crystallization process development Webinar 23 February 2024, Online About the … cmc aspen basecamp