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美國Coldstream Laboratories Inc 
At Coldstream Laboratories Inc., we're seasoned at turning pharmaceutical development ideas into safe, pure, and effective clinical pharmaceutical dosage forms. Since 1986, we have completed more than 200 formulation development projects that led to clinical trials providing us extensive clinical manufacturing experience with both commercial product development and grant-funded projects from such sources as the National Institutes of Health. We are registered with the FDA and the Commonwealth of Kentucky Board of Pharmacy for the clinical manufacturing of pharmaceutical products. Our work represents a wide range of formulations, testing, and production for a broad spectrum of clients.

Our current manufacturing capabilities include semi-solids, solutions, suspensions, and lyophilized powder dosage forms. Coldstream Laboratories Inc. has a full-capabilities analytical laboratory with proven method validation experience yielding the most accurate results possible. Our Formulation Development Unit has experience with a wide range of drug substances and excipients. Our Quality Systems organization operates under a quality manual, a validation master plan, and standard operating procedures that comply with the FDA's cGMP Regulations. Our Quality group is also responsible for approval of final product Certificates of Analysis.

Our senior management has more than 100 years of pharmaceutical industry experience in preformulation, analytical, and formulation development, as well as Phase I to Phase III clinical and commercial manufacturing.

Our goals are to:
Deliver a high quality product to our customers.

Be available, flexible, and carry out projects in a timely manner.

Provide high-quality, cost-efficient services.

Respect our customer’s intellectual assets by maintaining a high level of confidentiality.

We welcome visits to our facilities in Lexington, Kentucky to conduct audits or to meet with our scientists.