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Posted by smithmorgan on September 23, 2024 at 12:35pm 0 Comments 0 Likes
Posted by smithmorgan on September 23, 2024 at 12:34pm 0 Comments 0 Likes
Posted by Steven on September 23, 2024 at 12:31pm 0 Comments 0 Likes
IZiel helps you to obtain US FDA and CE approvals for Class I, II & III Medical Devices. Our Regulatory Consultants in US, Europe and India have thorough knowledge of USFDA & MDR Requirements alongwith extensive experience in submissions and approvals. IZiel works with the company to develop comprehensive documents in compliance with the regulatory requirements.
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