White Paper Overview US FDA Part 11 in Title 21 of the Code of Federal Regulations (CFR), and its EU analog, Eudralex Chapter 4, Annex 11, describe the requirements for electronic records and electronic signatures for regulated pharmaceutical organizations. Released in 1997, 21 CFR Part 11 has been enforced since 1999. The intent of these guidelines is to ensure that all appropriate electronic records are attributable, legible, contemporaneous, original, accurate, and maintained with integrity. This white paper is a resource for users of Agilent VWorks Plus Automation Software version 14.1, AssayMAP Protein Sample Prep Workbench 4.0, and later versions whose organizations must comply with these regulations. VWorks Plus Automation Software controls liquid handling and plate manageme

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