Consultant for Risk Management File for a Class II Medical device

We are looking for a qualified person\consulting firm to prepare the Risk Management File for the Class II Medical device. We have all test report and document such as IEC test reports, Recognized Standard Reports, Non Clinical Data and BioMedical Conformity report. The file will be used for FDA 510(k) submission. Please let me know if any one can or know someone who can do this for us.

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