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Neonatal drug trials: impact of EU and US paediatric regulations

Authors

  • Claudia Pansieri Service de Pharmacologie Pédiatrique, AP-HP, Hôpital Robert Debré, Paris, France Laboratory for Mother and Child Health, Department of Public Health, IRCCS Istituto di Ricerche Farmacologiche ‘Mario Negri’, Milan, Italy PubMed articlesGoogle scholar articles
  • Maurizio Bonati Laboratory for Mother and Child Health, Department of Public Health, IRCCS Istituto di Ricerche Farmacologiche ‘Mario Negri’, Milan, Italy PubMed articlesGoogle scholar articles
  • Imti Choonara Academic Division of Child Health, Derbyshire Children's Hospital, University of Nottingham, Derby, UK PubMed articlesGoogle scholar articles
  • Evelyne Jacqz-Aigrain Service de Pharmacologie Pédiatrique, AP-HP, Hôpital Robert Debré, Paris, France Université Paris Diderot, Sorbonne Paris Cité, Paris, France INSERM, CIC1426, Hôpital Robert Debré, Paris, France PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Evelyne Jacqz-Aigrain, Department of Paediatric Pharmacology and Pharmacogénétics, Hôpital Robert Debré, 48 boulevard Serurier, Paris 75019, France; evelyne.jacqz-aigrain{at}rdb.aphp.fr
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Citation

Pansieri C, Bonati M, Choonara I, et al
Neonatal drug trials: impact of EU and US paediatric regulations
Archives of Disease in Childhood - Fetal and Neonatal Edition 2014;99:F438.

Publication history

  • Accepted April 7, 2014
  • First published May 3, 2014.
Online issue publication 
March 22, 2016

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