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Item ID 132816513 in Category: Business Opportunities - Other Business Ads

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Configuration Management for Medical Device


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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Target State: All States
Target City : All Cities
Last Update : Nov 25, 2024 3:46 AM
Number of Views: 10
Item  Owner  : izielgroup1
Contact Email: (None)
Contact Phone: (None)

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2024-11-25 (0.604 sec)