News
Xceleron and Crystal Pharmatech Announce Partnership to Improve Early Clinical Development Utilizing Absolute Bioavailability Trials and Solid-State Solutions
22 Jan 2013
This milestone further demonstrates Candoo's expertise in formulation and biopharmaceutics to achieve bioequivalence among different polymorphs and/or salts. For new chemical entities (NCE), it is useful to conduct bridging studies in late clinical stage where a more stable or favorable polymorph or salt is identified, or to show BE between clinical and commercial formulations as per regulatory requirements. For generics, this technique will help clients to speed up the development of first-to-file (Paragraph IV) products and get products launched sooner.
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