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Test Reporting

NeoMedix is expert at performing all necessary design verification and design validation testing for your new product. We can also design and actively participate in your pre-clinical testing and evaluations. And when the time comes, our staff is knowledgeable in writing test reports and providing technical information for Investigational Device Exemption (IDE) applications, Institutional Review Board (IRB) approvals, 510(k) Pre-Market Notification submissions and Pre-Market Approval (PMA) applications.

  15042 Parkway Loop, Suite A, Tustin, CA 92780, USA Tel 714-258-8355 Fax 714-258-8356