1. Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human useOJ L 121, 1.5.2001
2. WORLD MEDICAL ASSOCIATION DECLARATION OF HELSINKI. Ethical Principles for Medical Research Involving Human Subjects, Adopted June 1964, as amended, See http://www.wma.net/en/30publications/10policies/b3/17c.pdf (Last visited 6 September 2016)
3. The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline on Good Clinical Practice, See http://www.ich.org/products/guidelines/efficacy/efficacy-single/article/good-clinical-practice.html (Last visited 6 September 2016)
4. Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC Text with EEA relevanceOJ L 158, 27.5.2014, p. 1–76
5. 2005 évi XCV. törvényazemberialkalmazásrakerülőgyógyszerekrőlésegyéb, a gyógyszerpiacotszabályozótörvényekmódosításáról. http://mkogy.jogtar.hu/?page=show&docid=a0500095.TV