Producing quality components and assemblies is MRPC’s number-one consideration. Our quality system is continuously upgraded, both with employee training and state-of-the-art inspection equipment. MRPC is certified to ISO 13485:2016. We also offer FDA registration services for components we produce for medical device manufacturers.

MRPC's quality management system starts with initial customer discussions about component requirements. It continues through finalization of component design, mold construction and validation efforts including IQ-OQ-PQ activities.

Once production begins, every step of the manufacturing process is monitored and controlled – from lot control of raw materials to packing and shipping of finished product. MRPC manufactures and ships components to meet your product specifications, and we take pride in the number of our "ship to stock" customers.

System Controls

MRPC applies system controls throughout the entire product realization process, such as:

  • Document Control
  • Visual Control Plans
  • Problem Resolution
  • Customized Inspection
  • ECO Control
  • Cross-Functional Training
  • Customer Support
  • Analysis Reporting
  • CAPA
  • Audits
  • Contract Reviews
  • Calibration

Program Controls

Through planning, verifications and precise tracking/documentation of products, processes and services, our fluid program controls include:

  • IQ/OQ/PQ Validations
  • Statistical Analysis
  • Sampling Goals PPAP
  • Program Tracking
  • Team Environment
  • Metrology Analysis
  • Communication
  • First-article Testing


Provide your information and attach your design documentation.

Submit it to our Engineering Department who will evaluate and assist with your quote.


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