1. Guideline on the Use of Pharmacogenetic Methodologies in the Pharmacokinetic Evaluation of Medicinal Productshttps://www.ema.europa.eu/en/documents/scientific-guideline/guideline-use-pharmacogenetic-methodologies-pharmacokinetic-evaluation-medicinal-products_en.pdf
2. Pharmacogenomic information in drug labels: European Medicines Agency perspective
3. Concept Paper on Predictive Biomarker-Based Assay Development in the Context of Drug Development and Lifecyclehttps://www.ema.europa.eu/en/documents/scientific-guideline/concept-paper-predictive-biomarker-based-assay-development-context-drug-development-lifecycle_en.pdf
4. Reflection Paper on Pharmacogenomics in Oncologyhttps://www.google.com.hk/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&ved=2ahUKEwj-qIvE27nxAhVVhP0HHQhRC0IQFnoECAMQAw&url=http%3A%2F%2Fwww.nifds.go.kr%2FdrugGeneDB%2F2015%2Finclude%2Fdownload.jsp%3Fnb_sral_atch_info%3D368&usg=AOvVaw1OU17lkBAbK2ZY4XGVRAvp
5. REGULATION (EU) 2017/746 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCILhttps://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32017R0746