1. Regulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on Medicinal Products for Paediatric Use and Amending Regulation (EEC) No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation (EC) No 726/2004 (Text with EEA Relevance). OJ L 378, of 27 Dec 2006
http://data.europa.eu/eli/reg/2006/1901/oj
2. Paediatric Investigation Plans
https://www.ema.europa.eu/en/human-regulatory/research-development/paediatric-medicines/paediatric-investigation-plans
3. Clinical Trials
https://www.efpia.eu/about-medicines/development-of-medicines/regulations-safety-supply/clinical-trials/
4. Joint Evaluation of Regulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on Medicinal Products for Paediatric Use and Regulation (EC) No 141/2000 of the European Parliament and of the Council of 16 December 1999 on Orphan Medicinal Products. Part 1/6. SWD (2020) 163 Final. Commission Staff Working Document. Brussels: European Union
https://ec.europa.eu/health/sites/health/files/files/paediatrics/docs/orphan-regulation_eval_swd_2020-163_part-1.pdf
5. Study on Off-Label Use of Medicinal Products in the European Union. Brussels: European Union
https://ec.europa.eu/health/sites/health/files/files/documents/2017_02_28_final_study_report_on_off-label_use_.pdf