Coldstream Laboratories is your outsourcing partner for pharmaceutical development and small-volume parenteral manufacturing services. We combine individualized service with unparalleled speed and flexibility to develop and manufacture parenteral drug products in liquid and lyophilized dosage forms. Unique mobile isolator technology within our FDA-approved sterile manufacturing facility ensures product containment for potent and cytotoxic compounds and radiolabeled products. Our highly skilled staff supports all aspects of the drug development process, including analytical chemistry and pre-formulation / formulation development services. Our onsite microbiology lab offers method validation and routine micro testing services, either in conjunction with manufacturing activities or as standalone services. Contact us today to learn more about Coldstream Laboratories.
Coldstream Laboratories, Inc., is seasoned at turning pharmaceutical development ideas into safe, pure, and effective pharmaceutical dosage forms. Since 2007, we have delivered unique solutions to complex development and manufacturing projects.
We are dedicated to delivering high quality products to satisfy international standards for both clinical and commercial applications. We are resolute in our commitment to provide quality pharmaceutical products to patients.
Our regulatory history includes a successful FDA inspection and completion of numerous client audits.
Let our experience and state-of-the-art facilities help take your next pharmaceutical project from concept to the patient in record time.
We welcome visits to our facilities in Lexington, Kentucky to see firsthand how we can help make your project successful. Contact us to learn more about Coldstream Laboratories today!