Facility Validation / Qualification

Pharmaceutical facilities are required to comply with the FDA current Good Manufacturing Practices (cGMP) and other regulatory bodies.

Water Systems

  • Purified water USP
  • Water for injection , Reverse Osmosis
  • Deionization
  • Ozonation
  • Clean Steam

Compressed Air Validation

  • CO2
  • SO2
  • O2
  • Oil Mist
  • Non-Viable Participate Count
  • Dew Point
  • Water Vapor, Hydrocarbon
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