Dalton is a Health Canada approved, FDA registered, cGMP contract service provider of integrated chemistry, drug development and manufacturing services to the pharmaceutical and biotechnology industries. We accelerate drug development programs by integrating formulation, process development, and manufacturing of API and finished dose forms at a single location. Our client benefits by having fully optimized and scalable processes with reduced timelines and costs throughout all phases of development and manufacturing. Dalton provides cGMP manufacturing of solid dosage forms and sterile filling services to customers at virtually any stage of development (Phase I, II, III or small scale commercial). We have on-site cGMP fill finish capabilities for both sterile injectable liquids and sterile powders, and a solid oral dosage manufacturing suite for capsule products. We bring 30 years of experience to our client's projects and emphasize quality, speed and flexibility. Our ongoing commitment to our clients is reflected in CMO 2016 Leadership Awards in the categories of Quality, Reliability, Capabilities, Expertise, and Compatibility, including On-Time Delivery and Right First Time. In 2016 Dalton was certified as A Great Place to Work.