MPI offers a wide spectrum of services and expertise in scientific, professional, manufacturing, quality control, and regulatory fields in compliance with applicable cGMP/GLP regulations mandated by the FDA.

Services include formulation development, drug delivery design, analytical method development/validation, drug stability assessment, clinical supply manufacturing, labeling, packaging, and shipping. For small scale isolation, extraction, and purification of drug moieties, the company possesses state-of-the-art supercritical fluid (SCF) units. In addition, MPI provides documentation and regulatory support for DMF preparations as well as IND, NDA, and ANDA submissions.