Examples of using Mutual recognition procedure in English and their translations into Polish
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Medicine
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In December 2005, a Mutual Recognition Procedure(MRP) started with Spain acting as Reference Member State
The application for Mutual Recognition for Rigevidon was submitted to Denmark and the Mutual Recognition Procedure started on 30 April 2004.
Discussion In his response the Marketing Authorisation Holder(MAH)did not develop any further the preclinical argument already presented during the mutual recognition procedure.
A Mutual Recognition Procedure(MRP) was started based on the Marketing Authorisation granted by the Netherlands with fourteen Concerned Member States.
decentralised procedure, mutual recognition procedure and national procedure)
Having in mind speeding up of EU cooperation procedure as regards review of BCR by personal data protection authorities, mutual recognition procedure has been agreed.
In March 2006 an application for a marketing authorisation for this vaccine was submitted, following a repeat use mutual recognition procedure, with Germany acting as Reference Member State.
Competent authorities of Member States that have issued national authorisations for the same biocidal product under the mutual recognition procedure shall examine whether the authorisation needs to be amended
European registration procedures, such as the Mutual Recognition Procedure(MRP) and Decentralized Procedure(DCP),
efficient functioning of the veterinary mutual recognition procedure.
was originally granted to AstraZeneca in The Netherlands on 6 November 2002 and a Mutual Recognition Procedure was started on 7 December 2002.
the applicant provided a copy of the original dossier as submitted in support of the application of a mutual recognition procedure, and any supplementary data submitted during the mutual recognition procedure and the referral procedure in CMD(v) thereafter.
The mutual recognition procedure applies for veterinary medicinal products already authorised in one Member State for which authorisation is requested in respect of two
The current procedure is a referral following a Mutual Recognition Procedure variation application, which concerned an extension of the indication for Prozac to include the treatment of major depressive episodes
plant protection product and for the same use in another Member State under the mutual recognition procedure, provided for in this subsection,
to as'the reference competent authority') may apply for a national authorisation of the biocidal product in another Member State under the mutual recognition procedure in sequence.
who have to apply different rules depending on whether they deal with a purely national authorisation, a mutual recognition procedure or a centralised authorisation.
of Directive 2001/83/EC as amended[1] the scope of this guideline is to set out in more detail in which exceptional cases a Member State concerned in a mutual recognition procedure as referred to in Article 28(2)
By defining in which exceptional cases the concerned Member State can refuse to recognise a marketing authorisation in a mutual recognition procedure, or a draft assessment report, a draft summary of products characteristics, and a draft of the labelling and package leaflet from the reference
the summary of product characteristics, the package leaflet and labelling from the reference Member State in a mutual recognition procedure or a draft assessment report, a draft summary of product characteristics