Superior Quality Assurance for Medical Device Manufacturing
Process Signature Verification provides the most detailed monitoring of your process possible.
A major medical device manufacturer used Sciemetric's PSV technology to build a case for the elimination of destructive pull tests on their welding process.
Science-level analysis is brought directly into the medical device manufacturing plant and leads to the following benefits:
- Objective proof of process compliance with specifications
- 100% verification of your medical device against known failure modes
- Reduced recalls through post-shipment reanalysis
- Reduced validation times
- Parametric release for reduced visual inspections
What is Process Signature Verification?
Process Signature Verification uses the change of physical parameters during a (manufacturing) process, to indicate the success or failure of that process, resulting in a 100% quality verification. In addition, Process Signature Verification also produces 100% process documentation and a parametric guide to root cause determination.
A process signature is a detailed description of the behavior of the physical parameters of a manufacturing process, such as force and distance in an assembly press operation.
Where can you use Process Signature Verification?
Many medical device manufacturing processes and quality tests can benefit from the insight generated by Sciemetric. The physical variables it measures and the calculated values it produces provide detailed information into the manufacturing processes. For instance, calculated 'work done' is often used to shorten verification time in press operations.
Download the datasheet on Sciemetric's Process Signature Verification for medical devices.
Results of Signature Verification