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.