Availability of age-appropriate paediatric formulations in the Netherlands: the need in daily clinical practice remains

Author:

van der Vossen AnnaORCID,Buljaç Sandra,Akçay Kadir,Brugma Jan Dietert,Vulto Arnold,Hanff Lidwien

Funder

Royal Dutch Pharmacist Association

Publisher

BMJ

Subject

General Pharmacology, Toxicology and Pharmaceutics

Reference30 articles.

1. . Regulation (EC) no 1901/2006 of the European Parliament and of the Council of 12 December 2006 on medicinal products for paediatric use (2006).

2. Bar-Shalom D , Rose K . Pediatric formulations: a roadmap 2016.

3. European Commission . State of Paediatric Medicines in the EU - 10 years of the EU Paediatric Regulation. Brussels 2017 26.10.2017. Contract No.: COM, 2017

4. European Medicines Agency with its Paediatric Committee . 10-Year report to the European Commission: general report on the experience acquired as a result of the application of the paediatric regulation. London: European medicines Agency, 2017. Available: https://ec.europa.eu/health/sites/health/files/files/paediatrics/2016_pc_report_2017/ema_10_year_report_for_consultation.pdf

5. Paediatric Committee . Revised priority list for studies on off-patent paediatric medicinal products. London: European medicines Agency, 2013. Available: https://www.ema.europa.eu/en/documents/other/revised-priority-list-studies-patent-paediatric-medicinal-products_en.pdf

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