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21 CFR PART-11 License Service
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|Type Of Services||Online|
|Cost||As per requirement|
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES).
21 CFR Part 11, the FDA's regulations for electronic documentation and electronic signatures.