Examples of using Mutual recognition procedure in English and their translations into Hungarian
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decentralised procedure, mutual recognition procedure and national procedure)
Nationally authorised veterinary medicinal products which have been subject to a referral procedure shall be transferred to a mutual recognition procedure.
In view of these concerns, during the Mutual Recognition Procedure, Belgium considered that a positive benefit/ risk balance had not been demonstrated and more robust evidence should be submitted
The current procedure is a referral following a Mutual Recognition Procedure variation application, which concerned an extension of
in Germany in January 2000 and subsequently in June 2000 in the EU and Norway via the mutual recognition procedure.
One cannabis-based medicine has been authorised through the mutual recognition procedure and marketed in 17 Member States, but no Member State has authorised
PL, RO, and SK,) through the Mutual Recognition Procedure with Hungary acting as the reference member state.
Rules should be established under the mutual recognition procedure to resolve any disagreements between competent authorities in a coordination group for mutual recognition and decentralised procedures for veterinary medicinal products"the coordination.
The application for UMAN BIG 180 IU/ ml solution for injection was submitted through the Mutual Recognition Procedure, on the basis of the marketing authorisation granted by the RMS(Italy) on the 2nd of June 1979.
inform the applicant of the possibility to submit an application under the mutual recognition procedure or the decentralised authorisation procedure. .
years of its implementation, to anticipate problems with the upcoming authorisation and mutual recognition procedure, and to update and adapt the instrument to recent policy developments.
Crestor(10 to 40 mg) was originally granted to AstraZeneca in The Netherlands on 6 November 2002 and a Mutual Recognition Procedure was started on 7 December 2002.
following concerns raised by Germany during a Mutual Recognition Procedure with Finland acting as Reference Member state.
following concerns raised by Germany during a Mutual Recognition Procedure with Finland acting as Reference Member state.
In March 2006 Intervet then submitted an application for a marketing authorisation for this vaccine following a repeat use mutual recognition procedure, with Germany acting as Reference Member State, for Denmark, Poland, Slovakia and Slovenia.
Information on the variations introduced since the grant of the marketing authorisation by decentralised procedure laid down in Article 49(7) or by mutual recognition procedure laid down in Article 52(8);
whether it is a national authorisation, mutual recognition procedure or centralised procedure for a medicinal product.
who have to apply different rules depending on whether they deal with a purely national authorisation, a mutual recognition procedure or a centralised authorisation.
to pre-empt problems with the upcoming product authorisation and mutual recognition procedure, and to update and adapt the instrument to recent policy developments.
This procedure is a referral following a Mutual Recognition Procedure concerning the above variation application which was submitted for Actira film-coated tablets to Germany as Reference Member State(RMS) and the Concerned Member States(CMS) AT, BE, DK, EL, ES, FI, IT, LU, PT and SE on 5 December 2006.