VAI's Cleaning Agent Manufacturing Division has addressed the needs of the Pharmaceutical and Biotechnology industries by designing a complete range of cleaning agents and disinfectants for the Class 100 aseptic manufacturing area. VAI's SCMD products are used at over 500 pharmaceutical and biotechnology organizations worldwide.

VAI's SCMD manufacturing operations mirror Current GMP's and enforces the adherence completely to USP specifications for testing of all manufactured products. VAI is an EPA and FDA registered facility.

SCMD represents a majority of the square footage of the Malvern, PA facility and manufactures a complete range of cleaning agents and disinfectants that are used daily by Class 100 operations. All VAI manufacturing operations are completely validated and routinely revalidated to assure product integrity. VAI capabilities for manufacturing products include the ability to fill aerosol, bulk and unidose packages in a Class 100 aseptic filling operation. Our aseptic filling operations are coupled with the validated and proven ability to irradiate a final product. Assurances are taken in every aspect of SCMD concerning sterility and particulate removal.

SCMD has taken another advancing step in product quality assurance by incorporating USP Water for Injection (WFI) into some of our products. The established WFI systems in our new SCMD facility incorporate an added advantage to the manufacture of our products. The mission of VAI's SCMD is to provide either a pyrogen free product where desired or a pyrogen reduced product where raw materials that must be incorporated have the inability to be processed as pyrogen free.

SCMD has manufacturing capabilities to produce both VAI products and contract custom manufacturing designs. In recent years, VAI has been asked by many Pharmaceutical and Biotechnology operations to manufacture raw materials for use in their operation. VAI's SCMD uncompromising cGMP manufacturing style and our complete adherence to USP specifications has assured outside organizations that their products will not only be produced and tested as sterile, but moreover, their product will be completely documented and validated. VAI's SCMD is proud of our history and track record. VAI's SCMD has never encountered a sterility failure in 6 years of production.

SCMD Capabilities:

• Class 100 Aseptic Filling Suites
• Class 1,000 Manufacturing Areas
• Class 10,000 Manufacturing Areas