An Energetic, Experienced and Knowledgeable Partner. Cedarburg Pharmaceuticals develops and manufactures commercial and clinical APIs. What sets us apart from others in the field is our single-minded dedication to success. We develop synthetic processes with the support of our scale-up team from the very beginning. Our analytical method development and QC teams provide further support to our development chemists. Combine these teams with full cGMP compliance and QA oversight from day one and you get Cedarburg's incomparable track record. With multiple DMFs filed, we have a track record of succeeding. Our highly qualified and innovative management and technical staff solve tough assignments in process development, scale-up and manufacturing, and analytical method development. With DEA controlled substance permits for Schedule I through Schedule V and a strong history of cGMP compliance, including two successful PAI inspections, we are an experienced, dependable and nimble resource for our customers.