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In review: the life sciences regulatory regime in Netherlands

This article reviews the essential regulatory considerations surrounding medicines and medical devices in Netherlands, including clinical trials and marketing authorisations. ....

The Netherlands , Research Ethics Committee , Patent Centre Netherlands , European Medicines Agency , Dutch Ministry Of Health , Central Committee On Research Involving Human Subjects , Good Laboratory Practice , Classification Medicinal , Medicines Directive , Medicines Act , Commodities Act Decree , Animal Testing Act , European Clinical Trial Directive , Medical Scientific Reserach , Human Beings , Medical Devices Regulation , Central Committee , Research Involving Human Subjects , Medical Research Ethics Committee , European Medicines Directive , Medicines Evaluation Board , Therapy Medicinal Products , Supplementary Protection Certificate , Patent Centre , European Economic Area , Wholesale Distribution Authorisation ,