Many Oral Solid Dosage (OSD) and Over-The-Counter (OTC) drug 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.
VTI can help ensure that your processes, facilities, equipment and procedures adhere to GMP requirements (21 CFR Parts 210 and 211) and are validated according to regulatory (FDA) standards. VTI has validation expertise and experience for equipment used in the manufacture of OSD forms and OTCs: blenders, grinders, mills, fluid bed dryers, homogenizers, encapsulators, spray and film coaters, fillers, sealers and cappers.