Finished Pharmaceutical Product

Monitoring of microbiological quality in the pharmaceutical industry is an important criterion that is required to justify safe… (More)

Quality by design (QbD) has recently been introduced in pharmaceutical product development in a regulatory context and the… (More)

The synthesis of pharmaceutical products frequently involves the use of reactive reagents and the formation of intermediates and… (More)

The main obstacles that drugs meet when administered via the buccal route derive from the limited absorption area and the barrier… (More)

In human medicine, the defined daily dose is used as a technical measure of drug usage, which is independent of the variations in… (More)

Freeze Drying involves transfer of heat and mass to and from the product under preparation, respectively, thus it is necessary to… (More)

The molecular mobility of amorphous pharmaceutical materials is known to be a key factor in determining their stability… (More)

A number of studies in the literature support the use of fine aerosols of drug, inhaled at low IFRs to target peripheral airways… (More)

Purpose. To measure the molecular mobility of amorphous pharmaceutical solids below their glass transition temperatures (Tg… (More)

Medical, ethical, and societal concerns about costs, access, and quality of care are causing health care practitioners to… (More)