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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 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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Changes over time for: Article 61
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Article 61U.K.
[F11. One or more mock-ups of the outer packaging and the immediate packaging of a medicinal product, together with the draft package leaflet, shall be submitted to the authorities competent for authorising marketing when the marketing authorisation is requested. The results of assessments carried out in cooperation with target patient groups shall also be provided to the competent authority.]
2.The competent authority shall refuse the marketing authorization if the labelling or the package leaflet do not comply with the provisions of this Title or if they are not in accordance with the particulars listed in the summary of product characteristics.
3.All proposed changes to an aspect of the labelling or the package leaflet covered by this Title and not connected with the summary of product characteristics shall be submitted to the authorities competent for authorizing marketing. If the competent authorities have not opposed a proposed change within 90 days following the introduction of the request, the applicant may put the change into effect.
4.The fact that the competent authority do not refuse a marketing authorization pursuant to paragraph 2 or a change to the labelling or the package leaflet pursuant to paragraph 3 does not alter the general legal liability of the manufacturer [F1and] the marketing authorization holder.
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