Examples of using Initial authorisation in English and their translations into Portuguese
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Financial
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Official
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Medicine
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Colloquial
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Ecclesiastic
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Ecclesiastic
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Computer
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Official/political
Operating conditions and initial authorisation.
They shall require investment firms to notify the competent authorities of any material changes to the conditions for initial authorisation.
This is true at all stages: initial authorisation, ongoing supervision and enforcement.
This means that it was not possible to obtain complete information about Coxevac at the time of the initial authorisation.
This means that it was not possible at the time of the initial authorisation to obtain complete information about Bovilis BTV8.
This means that it was not possible to obtain complete information about Zulvac 1 Ovis at the time of the initial authorisation.
The proposed Directive will harmonise the initial authorisation and operating conditions for investment firms established in the EU.
This means that it was not possible to obtain complete information about BTVPUR AlSap 1 at the time of the initial authorisation.
The initial authorisation to operate a nuclear installation is based on an appropriate safety analysis and a commissioning programme demonstrating that the installation, as constructed, is consistent with design and safety requirements;
Regular review of conditions for initial authorisation.
The relevant provisions encompass:-- conditions for initial authorisation, including organisational requirements( articles 4-14):-- general operating conditions including conflict of interest identification and management( articles 15-17);
This means that it was not possible to obtain complete information about Zulvac 1 Bovis at the time of the initial authorisation.
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 and, above all, guarantee a higher level of public health protection.
To ensure coherence those criteria should be consistent with the criteria applied in relation to shareholders and management in the initial authorisation procedure.
The principal implications of inclusion in ISD will be that:-- investment advisors become subject to initial authorisation and ongoing obligations established by the ISD.
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.
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.
It is therefore necessary to specify criteria for the supervisory assessment of shareholders and management in relation to a proposed acquisition or increase of a qualifying holding and a clear procedure for their application.To ensure coherence those criteria should be consistent with the criteria applied in relation to shareholders and management in the initial authorisation procedure.
They shall also ensure that competent authorities monitor that regulated markets comply at all times with the conditions for initial authorisation established under this Title.
The proposed Directive would update and harmonise the regulatory conditions with which investment firms must comply,at the time of initial authorisation and thereafter.
This broad coverage does not imply a« one size fits all»approach A common set of basic provisions will govern the conditions for the initial authorisation and organisation of all AIFM.
Organon submitted Implanon for a second renewal of the marketing authorisation through mutual recognition on the basis of the initial authorisation granted by the Netherlands on 25 August 1998.
The registration procedure for generic medicinal products needs to be simplified, so thatit 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.
An investment firm seeking authorisation to extend its business to additional investment services or activities orancillary services not foreseen at the time of initial authorisation shall submit a request for extension of its authorisation. .
In the case of investment firms which provide only investment advice, Member States may allow the competent authority to delegate administrative, preparatory orancillary tasks related to the review of the conditions for initial authorisation, in accordance with the conditions laid down in Article 482.
Article 9c(3) of Council Directive 70/524/EEC provides that 10 years after a substance has first been authorised,the findings of all or part of the evaluation of data and information contained in the dossier supplied for initial authorisation may be used for the benefit of other persons seeking authorisation to put that substance into circulation.
The investment firm shall provide all information, including a programme of operations setting out inter alia the types of business envisaged and the organisational structure, necessary to enable the competent authority to satisfy itself that theinvestment firm has established, at the time of initial authorisation, all the necessary arrangements to meet its obligations under the provisions of this Chapter.
The operator of the regulated market shall provide all information, including a programme of operations setting out inter alia the types of business envisaged and the organisational structure, necessary to enable the competent authority to satisfy itself that theregulated market has established, at the time of initial authorisation, all the necessary arrangements to meet its obligations under the provisions of this Title.
The data reporting services provider shall provide all information, including a programme of operations setting out inter alia the types of services envisaged and the organisational structure, necessary to enable the competent authority to satisfy itself that the data reportingservices provider has established, at the time of initial authorisation, all the necessary arrangements to meet its obligations under the provisions of this Title.
The new procedure outlined in Title III Chapter II(PUMA) for medicines with marketing authorisation that are not protected by a patent or supplementary protection certificate constitutes an important and viable innovation for available paediatric use marketing authorisation procedures.The possibility of following centralised procedures even if the initial authorisation for a pharmaceutical product for adults has been obtained through national procedures constitutes a genuine opportunity.