USFDA Consultants Medical Device | |
Medical Device Manufacturers require USFDA Approvals to sell their products in USA. USFDA differentiates product approvals in Class I, II &III depending upon the risk associated. The submissions include self-certification, 510(k) and PMA depending upon the class of the product.IZiel implements an Outcome-Based Delivery Model to provide complete solution from developing engineering documentation to receiving USFDA Approvals & establishment registrations thereafter. Our teams from USA & India collaborate to develop a Cost-Effective Model to complete USFDA Approvals for customers in USA, Europe and Asia. | |
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Target State: All States Target City : All Cities Last Update : Jul 16, 2024 7:10 AM Number of Views: 22 | Item Owner : izielgroup1 Contact Email: (None) Contact Phone: (None) |
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