Примери за използване на Authorisation procedure на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
only be launched if on the basis of the authorisation procedure the generating capacity being built
specific exceptions from the REACH authorisation procedure, the non-EEA company will have to decide whether to stop exporting the substance into the EEA market
only be launched if on the basis of the authorisation procedure the generating capacity being built
This is the first step in the REACH authorisation procedure which aims to control the risks from the most hazardous substances on the EEA market
Whereas, at the same time, transparency must be ensured at each step of the authorisation procedure, in full compliance with intellectual property rights,
reiterates Parliament's call for a reform of the EU's GMO authorisation procedure.
Current procedures are based on the principle that it is for the applicant to prove that the subject matter of an authorisation procedure complies with Union safety requirements given the scientific knowledge in its possession.
according to which factors were taken into account in the authorisation procedure.
The aim of this authorisation procedure is to ensure a high level of protection of human life
(16) Authorisations procedures are based on the principle that it is for the applicant to prove that the subject matter of an authorisation procedure complies with Union safety requirements given the scientific knowledge in its possession.
(28) It is necessary to establish a Community authorisation procedure for the placing on the market of GMOs,
the commercial exploitation of which entails a particularly onerous authorisation procedure, while ensuring the simplicity and transparency of the SPC regime.
If an applicant in the context of an authorisation procedure withdraws or has withdrawn an application,
(16a) A comparison of Union agencies shows that the Authority needs up to 55 months for an authorisation procedure or five times longer than the European Medicines Agency(EMA).
The aim of the authorisation procedure established at European level is to ensure a high degree of protection of human life
A new Regulation on biocidal products applying from 1st September will significantly increase the safety and simplify the authorisation procedure of biocides used and placed on the market in the EU.
the 1st of September will significantly increase the safety and simplify the authorisation procedure of biocides used and placed on the market in the EU.
Calls on the Commission to suspend any implementing decision regarding applications for authorisation of GMOs until the authorisation procedure has been revised in such a way
The Agency should provide advice on the prioritisation of substances to be made subject to the authorisation procedure, to ensure that decisions reflect the needs of society as well as scientific knowledge and developments.
An authorisation procedure for clinical trials which will allow for a fast