Voorbeelden van het gebruik van A marketing authorisation in het Engels en hun vertalingen in het Nederlands
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Medicine
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Programming
The holder of a marketing authorisation for the medicinal products covered by this Regulation should be established in the Community.
A marketing authorisation may be granted subject to one or more of the following conditions.
It should likewise not apply to homeopathic medicinal product eligible for a marketing authorisation or for a registration under Directive 2001/83/EC.
The European Commission granted a marketing authorisation valid throughout the European Union for Apidra to Sanofi-Aventis Deutschland GmbH on 27 September 2004.
The holder of a marketing authorisation for medicinal products covered by this Regulation must be established in the Community.
The European Commission granted a marketing authorisation valid throughout the European Union for ProMeris Duo to Fort Dodge Animal Health on 19 December 2006.
The European Commission granted a marketing authorisation valid throughout the European Union for Cerezyme to Genzyme Europe B. V. on 17 November 1997.
The European Commission granted a marketing authorisation valid throughout the European Union, for Rheumocam to Chanelle Pharmaceuticals Manufacturing Ltd. on 10.01.2008.
Which were the major concerns that lead the CVMP to recommend the refusal of a marketing authorisation?
The European Commission granted a marketing authorisation valid throughout the European Union for Onsior to Novartis Animal Health UK Ltd on 16.12.2008.
Belgium and Norway could not agree with granting a marketing authorisation.
Methoxasol-T was authorised through a national procedure in the Netherlands in 1999 but a marketing authorisation was refused in Germany in 2001.
The European Commission granted a marketing authorisation valid throughout the European Union, for Cortavance to Virback S. A. on 09/ 01/ 2007.
This part also regulates the‘protection period' applying to technical documentation submitted in order to obtain or amend a marketing authorisation.
The European Commission granted a marketing authorisation valid throughout the European Union for IVEMEND to Merck Sharp& Dohme Ltd on 11 January 2008.
The European Commission granted a marketing authorisation valid throughout the European Union, for Prac-tic to Novartis Sanidad Animal on 18.12.2006.
Article 40(3)(a) MPA allows pharmacists to prepare and supply medicinal products without a marketing authorisation.
safety data are already sufficient to support a marketing authorisation of Sativex.
The CHMP normally takes up to 90 days to adopt an opinion after it has received an application for a change to a marketing authorisation.
The European Commission granted a marketing authorisation valid throughout the European Union, for Reconcile to Eli Lilly and Company Ltd on 08.07.2008.
