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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
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