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Process and Cleaning Validation
VSI provides process validation for Medical Device, Pharmaceutical, and Biotechnology manufacturing processes. Our professionals can facilitate your process validation needs from development to full-scale manufacturing ensuring compliance with cGMP/QSR regulations and good business practices. VSI can assist with:
  • Process Development Reports and Evaluations
  • Scale-up and Technology Transfer
  • Design Reviews
  • Process Performance Qualifications
  • Product Performance Qualifications
  • Process Validation
  • Sampling Plans, Statistical Process Control and
  • Data Trending Analysis
  • Cleaning Validation Master Plans
  • Cleaning Validation Protocols
  • Swab Recovery and Method Validation Protocols

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Validation and Technical Services

Quality Systems Services

Laboratory Services