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.