Azopharma provides full product development and stand-alone services for the pharmaceutical, biotech and medical device industries. From preclinical to late phase development projects, Azopharma excels at meeting project deadlines while maintaining industry leading quality standards.
Our product development services include:
Our goal at Azopharma is to help maximize your financial resources by accelerating your timelines. Our proprietary Phase I Express process is designed to accelerate your drug development by leveraging our ability to manage the execution of multiple projects along parallel timelines.
Phase I Express begins with the synthesis of your NCE followed by its characterization, preformulation development and qualification of the necessary analytical techniques, assuring proper identification, quality and purity.
Azopharma provides formulation services in a variety of dosage forms and in support of preclinical and clinical studies. Starting with Phase I, we can manufacture your clinical trial material as well as conduct the clinical trials, including analytical support. Concurrently, we can provide CMC analytical services including stability studies.
Finally, Azopharma provides a variety of specialty and stand-alone services to support your product development efforts. We specialize in handling cytotoxic and potent compounds and have vigorous controls to insure safe and proper handling. Other specialty services include respiratory services for MDIs and DPIs and drug delivery technology for customized release profiles and poorly soluble drugs.
24-Jan-2008 - KBI Biopharma, Helix BioMedix and Azopharma have all recently announced new contract manufacturing news.
19-Nov-2007 - Contract pharmaceutical development company Azopharma has carved out its drug delivery segment into a new company, APIcross Drug Delivery Technologies.
26-Sep-2006 - Chemir Analytical Services, the new owner of Gateway Chemical Technology, has renamed the custom chemical analysis business IQsynthesis in a revamp effort.