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Cd formulation is a leading provider of enhanced bioavailability services, helping clients address low solubility, bioavailability, and dissolution rate issues in new chemical entities. Their services include ph modification, drug salt formation, drug pegylation, and precursor drug design. With experienced technicians, state-of-the-art equipment, and long-term expertise, cd formulation ensures fast time-to-market and reliable results.
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Industry estimates indicate that over 80% of new chemical entities exhibit low solubility, low bioavailability, and/or low or inconsistent dissolution rates. Effectively addressing these drug solubility, bioavailability, and dissolution rate issues is critical to advancing compound development and providing patients with the therapeutic benefits needed for pharmaceutical products. The Enhanced Bioavailability services provided by CD Formulation make us a leader in addressing issues of low solubility, low bioavailability and dissolution rates. Our end-to-end enhancement solutions combine the full capability to take a compound from concept to commercialization, minimizing project complexity, timelines and risk. Fig.1 API Chemical Modification
We help our clients with the ultimate manufacturability of their drug products to avoid time-consuming reformulations and ensure fast time-to-market, offering the following services: