Packaging Formats

MPC has over 30 years of experience helping customers discover the highest quality and most cost-effective packaging solutions for their products. MPC delivers turnkey manufacturing and assembly solutions that will exceed customer expectations. We can design packaging, source materials, handle logistics and build to order. Contact us to see how we can help you.
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MPC works with companies at all stages of design, from concept to preexisting, in an effort to deliver the highest-quality products to market. Let MPC’s experienced design team assist you define, create and deliver innovative products/solutions, while dramatically decreasing time to market. MPC can provide full-service product design ranging from concept and product specification to manufacturing.
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  • Liquid Injection Molding
  • Millable Injection Molding
  • Transfer Molding
  • Compression Molding
  • Insert Molding
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Automation plays a key role in the handling and quality assurance of the final product. We have developed automatic handling,
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Automation cont'd...

in process vision systems and automatic packaging for ship-to-stock programs.

MPC provides a full range of regulatory assistance and support to medical device companies. We can help you develop and implement the most advantageous regulatory strategy for your medical device, and prepare and submit the necessary documents to regulatory agencies to obtain marketing clearance.

Our consultants have extensive product experience and skills in regulatory affairs and an in-depth understanding of FDA, Canadian, and European requirements for marketing medical devices. MPC consultants include former senior regulatory affairs personnel from industry, as well as former senior FDA officials who were responsible for the review and approval of new medical devices.

With the combined experience and technical skills of our consultants, we can assist both large and small companies in bringing their products to market in the most direct, cost-effective manner. We can handle single projects, supplement your existing staff for specific tasks, or provide complete regulatory support for your company.

Key Regulatory Services
  • Assess impact of regulatory environment and FDA policies
  • Design pre-clinical and clinical studies
  • Evaluate technical and clinical data
  • Communicate and meet with FDA
  • Investigational Device Exemption (IDE) applications
  • Pre-market notifications [510(k)s]
  • Pre-market approval (PMA) applications
  • Device reclassification petitions
  • Master files
  • Canadian device license applications
  • Technical files for EU marketing
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