Примери за използване на A marketing authorisation на Английски и техните преводи на Български
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The European Commission granted a marketing authorisation valid throughout the European Union for Porcilis AR-T DF to Intervet International B. V. on 16 November 2000.
The European Commission granted a marketing authorisation valid throughout the European Union, for Melovem on 7 July 2009.
Without prejudice to Article 71 of Directive 2001/82/EC, a marketing authorisation which has been granted in accordance with this Regulation shall be valid throughout the Community.
Emtricitabine/Tenofovir disoproxil Mylan received a marketing authorisation valid throughout the EU on 16 December 2016.
The European Commission granted a marketing authorisation valid throughout the European Union,
The European Commission granted a marketing authorisation valid throughout the European Union,
The European Commission granted a marketing authorisation valid throughout the European Union,
By way of derogation from Article 5(2), a marketing authorisation for a limited market shall be valid for a period of 5 years.
Emtricitabine/Tenofovir disoproxil Krka received a marketing authorisation valid throughout the EU on 9 December 2016.
The European Commission granted a marketing authorisation valid throughout the EU for Suvaxyn Circo+MH RTU on 6 November 2015.
Any medicinal product not appearing in the Annex may be granted a marketing authorisation by the Community in accordance with the provisions of this Regulation, if.
A marketing authorisation may only be granted to an applicant established in the Community.
The European Commission granted a marketing authorisation valid throughout the European Union for Elaprase to Shire Human Genetic Therapies AB on 8 January 2007.
Where a medicinal product is granted a marketing authorisation for a paediatric indication,
The objections raised by France should not prevent the granting of a marketing authorisation for Equibactin vet.
The European Commission granted a marketing authorisation valid throughout the European Union for ProteqFlu on 6 March 2003.
The applicant or the holder of a marketing authorisation shall be responsible for the accuracy of the documents and of the data submitted.
The European Commission granted a marketing authorisation valid throughout the European Union for Porcilis Pesti to Intervet International B.V.
The European Commission granted a marketing authorisation valid throughout the European Union, for Cortavance to
Sweden should not prevent the granting of a marketing authorisation.