I3CGlobal is the ONLY consulting company who takes up complete turnkey FDA 510(k) projects. We cover any type of medical devices anywhere in the world FDA 510 k .
Special features of I3CGlobal
We will not assist, we prepare 510k!!!
We provide service of US Agent!!!
Initial in-depth study of product and regulatory followed by overall guidance
Development of a Project Plan and confirmation of the specific deliverables.
Guidance on testing
Communicate to FDA regarding review comments
Support in implementing 21 CFR 820
Establishment registration
Listing of products with US FDA
Payment after completing every phase.
Any clarification and service request please fill up the enquiry form
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