Examples of using Reference member state in English and their translations into Swedish
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
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Programming
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Political
The competent authority in the reference Member State shall refer the points of disagreement without delay to the coordination group.
These Member States were not been able to reach an agreement in respect of the Mutual Recognition of the Marketing Authorisation granted by the Reference Member State.
Under the present system, the Member States must recognise an initial authorisation granted by the reference Member State.
decentralised procedure with Sweden as Reference Member State(RMS), the latest approved English SmPC is already available at the MPA and can be attached to the certificate.
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.
Decisions concerning variations related to safety issues shall be implemented within a timeframe as agreed between the competent authority of the reference Member State and the holder in consultation with the other competent authorities of the Member States concerned.
Norway or Iceland is also recognised in other countries based on a marketing authorisation granted by a Reference Member State RMS.
On the request of the competent authority in the reference Member State referred to in paragraph 3, the marketing authorisation holder shall provide the coordination group with a summary that specifies the
The Reference Member State were Estonia,
A formal statement that the plant protection product is identical to that authorised by the reference Member State;
The reference Member State shall prepare
The competent authority of the reference Member State shall inform the other competent authorities of the Member States concerned to this effect.
A list of the Member States concerned and an indication of the reference Member State for the medicinal product under consideration;
The competent authority in the reference Member State shall without delay forward that request and the detailed grounds to the coordination group.
The competent authority in the reference Member State shall make the assessment report publicly available, after deleting any commercially confidential information.
In the new agreed timetable the concerned Member States send their comments to the reference Member State within 50 days instead of 55 days.
Within 90 days of receipt of a valid application, the reference Member State shall prepare an updated assessment report for the veterinary medicinal product.
These Member States were not able to reach an agreement in respect of the Mutual Recognition of the Marketing Authorisation granted by the Reference Member State.
The competent authority of the reference Member State shall evaluate these data