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* 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>{{cite |chapterurl=http://ec.europa.eu/health/files/eudralex/vol-4/pdfs-en/2005_10_chapter_6_en.pdf |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=Revised 1 June 2006 |page=3}}</ref>
=== Document approval ===
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