Examples of using Reference competent in English and their translations into Romanian
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
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Programming
The reference competent authority shall also inform the other concerned Member States.
A reference to the national authorisation granted by the reference competent authority;
The reference competent authority shall be responsible for the evaluation of the application.
The receiving competent authority shall authorise the biocidal product concerned under the same conditions as the reference competent authority.
The names of the reference competent authority and of the other concerned Member States.
The applicant shall submit to the competent authorities of the other concerned Member States an application for mutual recognition of the authorisation for which it has applied to the reference competent authority.
A reference to the report of the reference competent authority summarising the conclusions of its assessment and the reasons for authorising the biocidal product.
If the applicant seeks to receive national authorisations for a biocidal product in more than one Member State in parallel,he shall submit to a reference competent authority of his choice an application containing.
The reference competent authority shall, within one month after the receipt of an application referred to in paragraph 1, validate the application if it complies with the following requirements.
Within four months after receipt of the documents referred to in paragraph 6, the competent authorities of other concerned Member States shall approve the assessment report and the summary of the product characteristics, andshall inform the reference competent authority accordingly.
The reference competent authority shall, within one month after the receipt of the additional information, determine whether the additional information submitted is sufficient to validate the application.
The holder of a national authorisation for a biocidal product granted by a competent authority in accordance with Article 15(hereinafter referred 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.
The reference competent authority shall reject the application if the applicant fails to submit the requested information within the deadline and shall inform the applicant and the other concerned Member States thereof.
If the Commission decision dismisses the grounds presented for refusing or restricting the national authorisation the competent authority that proposed to refuse to recognise the authorisation, orto restrict the authorisation, shall without delay authorise the biocidal product concerned in accordance with the national authorisation issued by the reference competent authority.
If the reference competent authority, on the basis of the validation made pursuant to paragraph 3, considers that the application is complete, it shall without delay inform the applicant and the other concerned Member States.
The authorisation can be given through three main ways: the‘centralised' procedure(a single authorisation process, a single authorisation valid in the whole EU);the‘mutual recognition' procedure(one Member State acting as a reference competent authority and carrying the evaluation for the other concerned Member States); and the‘purely national' procedure(one evaluation and authorisation per Member State).
The reference competent authority and the competent authorities of the other concerned Member States shall authorise the biocidal product on the basis of the approved assessment report and the summary of the biocidal product characteristics within one month after the end of the period referred to in paragraph 7.
The reference competent authority shall evaluate the information referred to in paragraph 1 and prepare a report summarising the conclusions of its assessment and a draft of the summary of the biocidal product characteristics within 12 months from the receipt of a valid application and shall communicate the report and the draft summary to the competent authorities of other concerned Member States and the applicant.
Therefore, it is necessary to replace throughout the text any reference to competent authorities in charge of the registration and supervision by a reference to ESMA.
Therefore, it is necessary to replace throughout the text any reference to competent authorities in charge of the registration and supervision of credit rating agencies by a reference to ESMA.
For this purpose, any reference to competent authorities and river basin districts shall be taken as references to the competent authorities and unit of management referred to in this Article.