Manufacturing and Transfers

CRI takes a team approach to transferring manufacturing lines into our facility. We assign a dedicated Program Manager at the start, to ensure all deliverables are documented and tracked. We focus on improving process and product during the transfer, resulting in lower costs and improved quality. CRI also minimizes the effort for our customers, making transfers seamless and smooth.

  • Class 8 cleanroom facility
    • 1920 square feet
    • ISO certified
  • Controlled environment
    • all production working areas
  • Lean manufacturing
    • maximizing customer value while minimizing waste
    • resulting in lower and controlled costs
      • Evaluate all aspects of process
      • Eliminate non-value added steps
      • Minimize process steps
      • Less human efforts, less space, less cue times, less waste, less inventory
      • Single piece flow
      • Reduces errors and improves visualization of process
      • Reduces errors and improves visualization of process
  • Visual manufacturing
    • Organized work centers and processes
    • Indicators at all stages of process for status
  • Fully integrated MRP system
    • Utilizing M2M software for all aspects of business
    • Bar coding
    • Automated manufacturing processes and cost analysis by product
  • Document Control
    • Our document control process includes all regulatory requirements for this critical area of our Quality Management System. This includes lock out of documents pending changes, to ensure implementations are compliant and that errors are prevented. The final stage of document control includes training and effectiveness measurement.
      • Fully implemented change control system for all documents for a fully compliant Quality Management System
      • Device Master Records (DMR)
      • Device History Records (DHR) for all lots manufactured
      • Document control process tracked for quick change turn around
      • Standards library always kept up-to-date
Manufacturing and Transfers