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Data Aquisition

Validation is a mandatory requirement of the FDA's Quality System Regulations as a way of managing the quality of the process. Our staff is expert in developing and performing testing programs to support design verification and validation, critical inputs to the successful design review and control process. A particularly powerful capability is NeoMedix's extensive use of state-of-the-art computerized data acquisition systems, a superior means for generating, documenting, analyzing, and reporting test results.

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