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Directive 2001/83/EC of the European Parliament and of the CouncilShow full title
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
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Revised version PDFs
- Revised 26/07/20194.19 MB
- Revised 28/01/20191.47 MB
- Revised 16/11/20121.37 MB
- Revised 21/07/20111.88 MB
- Revised 20/01/20111.76 MB
- Revised 05/10/20090.46 MB
- Revised 20/07/20090.45 MB
- Revised 30/12/20080.45 MB
- Revised 21/03/20080.44 MB
- Revised 26/01/20070.44 MB
- Revised 30/04/20040.42 MB
- Revised 01/07/20030.38 MB
- Revised 08/02/20030.31 MB
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Article 64U.K.
Where the provisions of this Title are not complied with, and a notice served on the person concerned has remained without effect, the competent authorities of the Member States may suspend the marketing authorization, until the labelling and the package leaflet of the medicinal product in question have been made to comply with the requirements of this Title.
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