Datasheet

Ziflow Security and Compliance whitepaper

Get an overview of Ziflow’s security and privacy practices as they pertain to the specific requirements noted in Title 21, Part 11 of the Food and Drug Administration’s Code of Federal Regulations, which establishes the United States Food and Drug Administration (FDA) requirements on electronic records and electronic signatures.

This document details Ziflow’s role as a software provider as it pertains to each individual edict contained within this set of requirements, as well as any responsibilities that the customer must hold in order to maintain adherence to these federal regulations.

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