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21 CFR part 11 outlines rules for electronic records and signatures to be equivalent to paper records. This means you can use an electronic system instead of paper documentation to comply with FDA regulations. The focus of this video is on the requirements for electronically signing documents, including the need for personal login credentials and verification of user identity. Additionally, there are requirements for electronic record-keeping, such as system validation and audit trails, which will be covered in another video. Users must use two components (username and password) for electronic signature.