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Posted by smithmorgan on September 23, 2024 at 7:03am 0 Comments 0 Likes
Posted by smithmorgan on September 23, 2024 at 7:03am 0 Comments 0 Likes
Posted by smithmorgan on September 23, 2024 at 7:03am 0 Comments 0 Likes
Posted by Prajakta on September 23, 2024 at 7:02am 0 Comments 0 Likes
IZiel works in collaboration with your team to develop the complete Design History File (DHF) including requirements management, risk management, process validations and software validations using robust design controls process and quality system procedures. Thereafter, IZiel team works with their regulatory team in USA to complete the submissions (510k or PMA) and resolve queries, if any, from USFDA.
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