USDeviceAgent.com provides a complete US Agent service and regulatory advice on medical devices in the medical, pharmacuetical, optical, contract manufacturing / sterilization and surgical industries. The US Device Agent provides information on FDA requirements for foreign products within FDA guidelines.
21 CFR Parts 207, 607, and 807
Section 417 FDA Modernization Act of 1997
Company’s Keywords:
medical device, fda, regulatory consulting
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