DPT will expedite your drug development program through effective, efficient production of clinical trial materials. Our drug formulation development scientists and pharmaceutical manufacturing teams work directly with you and/or your contract research organization (CRO) to assist with technology transfers for later-phase clinical trial supplies, registration batches, and commercial launch.
DPT’s integrated CDMO services and in-depth experience with technology transfers ensure that clinical trial manufacturing processes pass seamlessly to commercial-scale production. We have extensive experience in handling the development and cGMP manufacturing of liquids, lotions, nasal spray formulations, and many other dosage forms. Additionally, we provide packaging identification, compatibility assessments, and other related tasks, as well as scale-up estimates when your product moves into commercial cGMP manufacturing.
Clinical Trial Supply Solutions
- cGMP batch sizes from 0.3 kg
- Extensive packaging capabilities
- Phase I–III clinical materials