Načela in podrobne smernice dobre proizvodne prakse iz prejšnjega člena so določena in objavljena v naslednjih publikacijah, ki jih je sprejela Evropska komisija:
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"The Rules Governing Medicinal Products in the European Union, Volume 4 – Good Manufacturing Practices, Medicinal Products for Human and Veterinary use, 1998 Edition, European Commission, Directorate General III – Industry, Pharmaceutical and Cosmetics" z vsemi dopolnitvami, spletna stran http://dg3.eudra.org/F2/eudralex/ index.htm",
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"Compilation of Community Procedures on Inspections and Exchange of Information, Published on behalf of the European Commission by the EMEA (European Medicines Agency), spletna stran http://www.emea.eu.int/inspections/ gmpcompproc.html.