1. European Medicine Agency. Good practice guide on recording, coding, reporting and assessment of medication errors. [cited 2016 May 05]. Available from: http://www.ema.europa.eu/docs/en_GB/document_library/Regulatory_and_procedural_guideline/2015/11/WC500196979.pdf.
2. European Medicine Agency. G Good practice guide on risk minimisation and prevention of medication errors. [cited 2016 May 05]. Available at: http://www.ema.europa.eu/docs/en_GB/document_library/Regulatory_and_procedural_guideline/2015/11/WC500196981.pdf.
3. Legislative Decree No. 219 of April 24, 2006 on the Implementation of Directive 2001/83/EC (& Subsequent Amending Directives) on the Community Code on Medicinal Products for Human Use, and the Directive 2003/94/EC. Rome (Italy): Italian government; Gazzetta Ufficiale n. 142; 2006 Jun 21.
4. Assessment of a New Instrument for Detecting Preventable Adverse Drug Reactions