Part 11, Electronic Records; Electronic Signatures - Scope and Application: Guidance for Industry From Food and Drug Administration (FDA) πΊπΈ This document is a guidance for the industry on the scope and application of Part 11, covering topics like compliance, electronic submissions, and good clinical practice. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on September 29, 2023 Other (Public Domain) 0 reuses 0 favorites