FDA Regulation Title 21 CFR Part 11 (also referred to as 21 CFR 11), Electronic Records/Electronic Signatures, is that the a part of the Code of Federal Regulations that establishes the us Food and Drug Administration (FDA) regulations on electronic records and electronic signatures. Specifically, 21 CFR 11 defines the wants for submitting documentation in… Continue reading
Category: 21 cfr part 11
Protect Your Records With FDA 21 cfr part 11
21 cfr part 11 , Data protection is a very comprehensive subject that involves updating organizations, backups, access controller and others. In the context of data protection, we will present in this post the FDA CFR 21 Part 11. This standard was specifically designed to provide guidelines that seek to ensure the security and legitimacy… Continue reading