Examples of using Reference member in English and their translations into Slovak
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Medicine
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Colloquial
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Official
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Financial
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Ecclesiastic
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Official/political
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Computer
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Programming
package leaflet of the Reference Member State.
To this end, the marketing authorisation holder shall request the reference Member State either to prepare an assessment report in respect of the veterinary medicinal product or, if necessary, to update any existing assessment report.
submitted to the National Competent Authority of the Reference Member State within three months of approval.
The procedure shall then be considered to be closed and the reference Member State and each of the Member States concerned shall authorise the biocidal product in accordance with Article 33(3) or 34(6) as appropriate.
with Germany acting as Reference Member State, for Denmark,
amended by Directive 2004/27/EC, Member States have only 30 days from the assessment by the reference Member State to grant marketing authorisations.
the coordination group shall take into account whether any Member State is acting as a reference Member State, in accordance with Article 28(1).
In the latter case, he shall certify that the summary of the product characteristics proposed by him in accordance with Article 14 is identical to that accepted by the reference Member State in accordance with Article 25.
plant protection product concerned under the same conditions, including classification for the purpose of Directive 1999/45/EC, as the reference Member State.
send it a copy of the authorization granted by the reference Member State.
If, within 60 days of the communication of the points of disagreement, the Member States reach an agreement, the reference Member State shall record the agreement,
each Member State shall recognize the marketing authorization granted by the reference Member State within 90 days of receipt of the application
For mutual recognition in parallel, the company can submit an application for product authorisation in one Member State(called the reference Member State) and simultaneously ask other countries to recognise the authorisation as soon as it is granted.
For mutual recognition in parallel, the company can submit an application for product authorisation in one Member State(called the reference Member State) and simultaneously ask other countries to recognise the authorisation as soon as it is granted.
Although the Reference Member State concluded that the objections raised had been resolved,
Germany, reference member state in the decentralised procedure,
The Reference Member State was Sweden
The Reference Member State was Netherlands
it shall forthwith inform the applicant, the reference Member State which granted the initial authorisation,
a detailed statement of the reasons shall be provided to the reference Member State, the other Member States