Pediatr Endocrinol Rev
September 2011
The story of the founding of ESPE and of its first annual meetings as told by founding members.
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October 2010
The Dutch Medical Research Involving Human Subjects Act (WMO) limits non-therapeutic research in children by means of the absolute requirement of negligible risk and minimal burden. The European Clinical Trials Directive, however, allows clinical research with medicinal products in children when, among other requirements, the investigation has any direct benefit for the group of patients involved. In addition, pain, discomfort, fear and other anticipated risks should be minimised.
View Article and Find Full Text PDFNed Tijdschr Geneeskd
February 2010