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Agnès Saint-Raymond

Showing results (1-10 of 9) with videos related to

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Paediatric Respiratory Reviews|February 9, 2005
Development of medicines for children in Europe: ethical implicationsAgnès Saint Raymond, Daniel Brasseur
Paediatric Drugs|January 9, 2009
The European paediatric initiative: 1 year of experienceAgnès Saint-Raymond, Nathalie Seigneuret
Therapeutic Innovation & Regulatory Science|May 2, 2018
What to Know About Medicines With New Active Ingredients Approved in FY 2016 / 2016 in Japan and EU: A Brief Comparison of New Medicines Approved in Japan and the EU in 2016Hideyuki Kondo, Agnès Saint-Raymond, Naoyuki Yasuda
Expert Review of Clinical Pharmacology|March 24, 2015
White spots in pharmaceutical pipelines-EMA identifies potential areas of unmet medical needsMarisa Papaluca, Martina Greco, Enrico Tognana, et al.
Archives of Disease in Childhood|November 7, 2015
Usage of unpublished paediatric dataAgnès Saint-Raymond, Benjamin Pelle, Cosimo Zaccaria, et al.
Expert Review of Clinical Pharmacology|February 8, 2022
WHO collaborative registration procedure using stringent regulatory authorities' medicine evaluation: reliance in action?Alexandra Vaz, Mariana Roldão Santos, Luther Gwaza, et al.
Trials|November 21, 2018
Adaptive designs in clinical trials: from scientific advice to marketing authorisation to the European Medicine AgencyOlivier Collignon, Franz Koenig, Armin Koch, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 16, 2010
Guidance for clinical trials for children and adolescents with chronic hepatitis CStefan Wirth, Deirdre Kelly, Etienne Sokal, et al.
Transgenic Research|July 22, 2017
Fostering responsible research with genome editing technologies: a European perspectiveHervé Chneiweiss, François Hirsch, Lluis Montoliu, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Paediatric Respiratory Reviews|February 9, 2005
Development of medicines for children in Europe: ethical implicationsAgnès Saint Raymond, Daniel Brasseur
Paediatric Drugs|January 9, 2009
The European paediatric initiative: 1 year of experienceAgnès Saint-Raymond, Nathalie Seigneuret
Therapeutic Innovation & Regulatory Science|May 2, 2018
What to Know About Medicines With New Active Ingredients Approved in FY 2016 / 2016 in Japan and EU: A Brief Comparison of New Medicines Approved in Japan and the EU in 2016Hideyuki Kondo, Agnès Saint-Raymond, Naoyuki Yasuda
Expert Review of Clinical Pharmacology|March 24, 2015
White spots in pharmaceutical pipelines-EMA identifies potential areas of unmet medical needsMarisa Papaluca, Martina Greco, Enrico Tognana, et al.
Archives of Disease in Childhood|November 7, 2015
Usage of unpublished paediatric dataAgnès Saint-Raymond, Benjamin Pelle, Cosimo Zaccaria, et al.
Expert Review of Clinical Pharmacology|February 8, 2022
WHO collaborative registration procedure using stringent regulatory authorities' medicine evaluation: reliance in action?Alexandra Vaz, Mariana Roldão Santos, Luther Gwaza, et al.
Trials|November 21, 2018
Adaptive designs in clinical trials: from scientific advice to marketing authorisation to the European Medicine AgencyOlivier Collignon, Franz Koenig, Armin Koch, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 16, 2010
Guidance for clinical trials for children and adolescents with chronic hepatitis CStefan Wirth, Deirdre Kelly, Etienne Sokal, et al.
Transgenic Research|July 22, 2017
Fostering responsible research with genome editing technologies: a European perspectiveHervé Chneiweiss, François Hirsch, Lluis Montoliu, et al.
Pageof 1