Many Oral Solid Dosage (OSD) facilities run multiple products in processing areas designed for quick turnaround without unacceptable risk of product exposure (i.e. dust and cross- contamination). Additionally, potent or toxic active ingredients are becoming increasingly common. Pharmaceutical Services Corporation can help you ensure that your processes and procedures adhere to GMP requirements (21 CFR parts 210 and 211) and your equipment is validated according to regulatory (FDA) standards.

Pharmaceutical Services Corporation has validation expertise for equipment used in the manufacture of Oral Solid Dosage forms. Blenders, grinders, fluid bed dryers, encapsulators, spray and film coaters, fillers, sealers and cappers.