1. PharmaWiki Medikamente und Gesundheit. Zusatzstoffe. https://www.pharmawiki.ch/wiki/index.php?wiki=Zusatzstoffe. Accessed 4 Apr 2022.
2. EDQM. European pharmacopoeia (Ph. Eur. 10.7). As of 1 April 2022.
3. EMEA/CHMP/QWP/396951/2006. Guideline on excipients in the dossier for application for marketing authorisation of a medicinal product—Revision 2. Effective since 01.01.2008. https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-excipients-dossier-application-marketing-authorisation-medicinal-product-revision-2_en.pdf. Accessed 4 Apr 2022.
4. EU Guideline on Excipients in the labelling and package leaflet of medicinal products for human use. Effective since 3/2018. https://www.ema.europa.eu/en/human-regulatory/marketing-authorisation/product-information/reference-guidelines/excipients-labelling. Accessed 4 Apr 2022.
5. EMA/CHMP/302620/2017 Rev. 1. Annex to the European Commission guideline on Excipients in the labelling and package leaflet of medicinal products for human use’ (SANTE-2017-11668). Effective since 11/2019. https://www.ema.europa.eu/en/documents/scientific-guideline/annex-european-commission-guideline-excipients-labelling-package-leaflet-medicinal-products-human_en.pdf. Accessed 4 Apr 2022.