Examples of using Authorisation and supervision in English and their translations into Swedish
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Section 1 Authorisation and supervision.
Competent authorities responsible for authorisation and supervision.
Authorisation and Supervision of CSDs.
Requirements concerning the authorisation and supervision of testing centres.
Authorisation and supervision of credit intermediaries.
Provisions concerning the authorities responsible for authorisation and supervision.
Authorisation and supervision of medicinal products for human use.
Life assurance is subject to official authorisation and supervision in each Member State.
Authorisation and supervision of veterinary medicinal products.
Testing centres directly operated by a competent authority shall be exempted from the requirements regarding authorisation and supervision.
Title III Authorisation and supervision of CCPs.
Both the subsidiary and its parent undertaking are subject to authorisation and supervision by the same Member State;
The authorisation and supervision of insurance intermediaries and other sellers of
To lay down Community procedures for the assessment, authorisation and supervision of genetically modified food and feed;
To enable Markets and Investment Firms to provide services through the single market on the basis of home country authorisation and supervision.
New financial products should be subject to authorisation and supervision by national and European banking authorities.
An event that will have an important effect on the EMEA was the announcement by the European Commission of its proposals to reform the European system for the authorisation and supervision of medicines.
form of proportionate requirements for the authorisation and supervision of such undertakings as investment firms within the meaning of this Directive;
organisational rules, and(2.3) the authorisation and supervision regimes of CSDs;
relying on national authorisation and supervision of CCPs, with a strengthened role for the college of supervisors;
the Council as regards information on medicinal products EU procedures for the authorisation and supervision of medicinal products.
Regulation No 1829/2003 lays down procedures for the authorisation and supervision of genetically modified food and feed, and also the labelling thereof.
establish branches in other Member States on the basis of home country authorisation and supervision.
Regulation 2309/93 makes provision for the evaluation of the Community procedures for the authorisation and supervision of medicinal products which entered into force in 1995.
raise concerns about possible new risks to the orderly functioning of markets, even more so that not all HF traders are subject to authorisation and supervision under the MiFID.
Regulation(EC) No 1829/2003 lays down Community procedures for the authorisation and supervision of genetically modified food and feed and for the labelling of such food and feed.
establish branches in other Member States on the basis of home country authorisation and supervision.
The new European regulations establish common requirements for the authorisation and supervision of hedge funds, but they are far
No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency- C6-0517/2008.
Proposals for the revision of the European system for the authorisation and supervision of medicines were transmitted to the European Parliament