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