Medicinal Products In The European Union: The Legal Framework For Medicines For Human Use

Author (Corporate)
Publisher
Series Title
Series Details April 2015
Publication Date 20/04/2015
ISBN 978-92-823-6827-5
EC QA-01-15-230-EN-N
Content Type

A high level of protection for human health is a central objective of European Union (EU) public health policy. To guarantee this objective, high standards of quality and safety for medicinal products are essential.

Although pharmaceuticals are primarily regulated at the national level by the Member States, there is a large body of EU legislation in the field.

Written by Nicole Scholz.
Source Link Link to Main Source http://dx.publications.europa.eu/10.2861/345854
Related Links
European Parliament: Directorate-General for Internal Policies of the Union: Publications available via the EU Bookshop http://bookshop.europa.eu/en/directorate-general-for-internal-policies-of-the-union-cbf.cKABstF7wAAAEjwYYY4e5K/
EP: EPRS: In-Depth Analysis, April 2015: Medicinal Products In The European Union: The Legal Framework For Medicines For Human Use http://www.europarl.europa.eu/RegData/etudes/IDAN/2015/554174/EPRS_IDA(2015)554174_EN.pdf
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