The experienced team of analytical chemists and formulation scientists at Coldstream will assist you in the early stages of drug development through Phase III and commercial manufacturing. Whether prepping for a NDA or ANDA submission, Coldstream's development team can provide you with solid analytical methods, robust formulations and reliable test results.
Our Analytical Research and Development, Formulation Development, and Analytical Quality Control laboratory areas are equipped with state-of-the art instrumentation as well as a special cytotoxic and potent handling area.
Additionally, our Quality Unit will provide all of the necessary regulatory assistance to support your project. We can help facilitate your submission and guarantee that your project is developed and registered in a timely and cost-efficient manner.