1. World Medical Association Declaration of Helsinki
2. European Council: 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;Off J Eur Union,2014
3. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use . ICH Harmonised Guideline: Integrated addendum to ICH E6(R1): Guideline for Good Clinical Practice E6(R2). London, England: European Medicines Agency, 2016.
4. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use . ICH Harmonised Guideline: ICH E11(R1) guideline on clinical investigation of medicinal products in the pediatric population. London, England: European Medicines Agency, 2017.
5. Future of clinical trials in the delivery room: time for pragmatism