Examples of using Reference member state in English and their translations into Hungarian
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Programming
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Official/political
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Computer
The applicant shall request one Member State to act as‘reference Member State' and to prepare an assessment report on the medicinal product in accordance with paragraphs 2 or 3.
The reference Member State shall prepare or update the assessment report within 90 days of receipt of a valid application.
The reference Member State shall prepare these drafts within 120 days of the receipt of a valid application
It shall inform the reference Member State which granted the initial authorization, the other Member
The reference Member State shall establish the agreement of all parties,
The applicant shall request one Member State to act as“reference Member State” and to prepare an assessment report on the medicinal product in accordance with paragraphs 2 or 3.
The original authorisation was granted by a Member State( reference Member State) which belongs to the same zone(see zonal procedure);
The applicant shall request one Member State to act as reference Member State and to prepare an assessment report in respect of the veterinary medicinal product in accordance with paragraphs 2 or 3.
The authorisation was granted by a Member State( reference Member State) which belongs to the same zone;
In June 2007 a mutual recognition procedure started with Germany as Reference Member State and 5 Concerned Member States. .
A Mutual Recognition Procedure(MRP) started on 22 September 2005 with Finland acting as Reference Member State and twelve Concerned Member States. .
started with Spain acting as Reference Member State and ten Concerned Member States. .
In June 2006 a Mutual Recognition Procedure started with The Netherlands as Reference Member State and six Concerned Member States. .
The authorisation was granted by a Member State( reference Member State) which belongs to the same zone; or.
The Reference Member State was Netherlands
The Reference Member State was Sweden
The Reference Member State was the United Kingdom
Although the Reference Member State concluded that the objections raised had been resolved,
If there is disagreement between one of the Member States concerned and the reference Member State, particularly if one of them considers that the medicinal product poses a risk for human
The Reference Member State was Ireland and the Concerned Member States were Belgium,