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Line 9: * When electronically produced, the documentation must be checked for accuracy<ref name=EUGMP4 /> * Free from errors<ref name=FDAGCP /><ref name=EC94>[http://ec.europa.eu/enterprise/sectors/pharmaceuticals/files/eudralex/vol-1/dir_2003_94/dir_2003_94_en.pdf European Commission Directive 2003/94/EC. (Article 9)]</ref> * For some types of data, it is recommended that records are in a format that permits trend evaluation<ref name=EUGMP6>{{citation \|chapter-url=~~http~~https://ec.europa.eu/health/sites/default/files/files/eudralex/vol-4/~~pdfs~~chapter4_01-~~en/2005_10_chapter_6_en~~2011_en.pdf \|chapter-format=pdf <!-- \|work=EudraLex --> \|title=The rules governing medicinal products in the European Union \|volume=Volume 4, EU Guidelines to Good Manufacturing Practice, Medicinal Products for Human and Veterinary Use. \|chapter=Part I, Chapter 6 Quality Control \|date=1 June 2006 \|page=3}}</ref> === Document approval ===

Good documentation practice: Difference between revisions