Examples of using Initial authorisation in English and their translations into Italian
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Official/political
The initial authorisation to operate a nuclear installation is based on an appropriate safety analysis
I therefore totally agree with the Commission's proposal to harmonise the procedures for authorising variations made to medicines, regardless of the initial authorisation procedure, as this simplification will streamline the entire system
Member States shall ensure that the competent authorities keep under regular review the organisational arrangements which investment firms have been required to put in place as a condition for initial authorisation.
allow for this extension, while avoiding the re-assessment of the application by all the Member States concerned which were involved in the initial authorisation of the clinical trial.
For the initial authorisation it involves only the Member States where the clinical trial is to be performed a mechanism would have to be set up to allow roll-out to additional Member States subsequently.
Common rules agreed since the 1970s include conditions for initial authorisation, on-going prudential supervision,
If the Commission decision confirms the initial national authorisation, the competent authority that proposed to refuse to recognise a national authorisation, or to recognise the national authorisation subject to certain conditions, shall without delay authorise the biocidal product concerned in accordance with the initial authorisation.
This Article provides that the rules laid down for initial authorisation must continue to be respected once the management company has started to carry out its activity.
applicant CCP has established, at the time of initial authorisation, all the necessary arrangements to meet its obligations set out in this Regulation.
Member States shall require that an investment firm authorised in their territory comply at all times with the conditions for initial authorisation established in Chapter I of this Title.
sponsors may have an interest to extend the clinical trial to an additional Member States after the initial authorisation of the clinical trial.
ancillary services not foreseen at the time of initial authorisation shall submit a request for extension of its authorisation. .
by the same procedure as the initial authorisation procedure.
we will want to- find out what has happened in the six months since our initial authorisation of those plans.
they should be subject to an authorisation procedure similar to the initial authorisation procedure.
it is possible to place generic medicinal products on the market directly upon expiry of the ten-year period following initial authorisation of the reference medicinal product.
number of elements that the competent authority may examine, so as to make it easier to obtain an entry-into-service authorisation in a Member State other than the one which issued the initial authorisation.
The initial authorisation should be granted for a period of 10 years subject,
ancillary tasks related to the review of the conditions for initial authorisation, in accordance with the conditions laid down in Article 482.
regulated market has established, at the time of initial authorisation, all the necessary arrangements to meet its obligations under the provisions of this Title.