"Since installing the SMART software we have never ever missed a process step, installed the wrong component, used the wrong equipment, used materials out of effectivity date, missed a measurement, performed the wrong test or allowed untrained people to perform work. In short we're not talking about Six Sigma or 99.9% acceptance rate but preventing all problems and achieving ZERO DEFECTS."
                                  Director Operations at Major Medical Device and Pharma Company

QCR can provide an immediate solution!

•     Forcing verification of regulatory compliance throughout your processes as they're performed
•     Produce real-time device, product and part history records
•     Eliminating mistakes and omissions 
•     Meet 21CFR Part 11 Requirements  
•     Reducing cost of goods manufactured (Including services)
•     Exceed 21CFR Part 820 requirements
•     Exceed ISO 9000-2000 Requirements
•     Improving customer satisfaction.
•     Increasing efficiency and productivity by at least 25%.
•     Reducing paperwork