Contact Us    Industry Related Links   Home   
 
 
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
 
 

About Us

Validation and Technical Services

Quality Systems Services

Laboratory Services