Sentence examples for further authorisations from inspiring English sources

Exact(2)

Further authorisations would be needed if that decision was ever taken, one US intelligence source said.

Classification and authorisations: The study protocol was submitted to the Spanish Agency of Drugs and Health Products (the competent authority) and classified as a 'postauthorisation study with design other than prospective follow-up' requiring no further authorisations (SPM-ACO-2014 01; 12 March 2014).

Similar(58)

Mr Annan stopped just short of reiterating a suggestion he made last week that military action against Iraq without further authorisation would be illegal or in violation of the UN Charter.

In those cases where the SEv process identifies a need for further regulation, authorisation requirements or restrictions might be initiated.

These documents were used to further obtain authorisation and administrative clearance from the divisional officers, district medical officers and, in the Bafut case, of the traditional ruler, in order to get the local consent to conduct fieldwork.

5 a. Member States may further liberalise the authorisation system for national regular services with regard to authorisation procedures and kilometre thresholds.

"When the protesters started to congregate together just before the proposed occupation it appears that Kennedy went much further than his authorisation.

The files of undisclosed evidence, the judges said, reveal Kennedy "was involved in activities which went much further than the authorisation he was given, and appeared to show him as an enthusiastic supporter of the proposed occupation of the power station and, arguably, an agent provocateur".

Assessing bioaccumulation is further required for the authorisation of chemicals in many national and international legislative frameworks.

During phase I of our audit vancomycin, carbapenems and third generation cephalosporins were not used regularly (not in our top 5 most commonly used antibiotics) and we concluded that the local formulary guidelines appeared to be respected without possible improvement with further formulary restriction and pre-authorisation [ 16- 18].

Olaratumab, manufactured by US-based pharmacompanyl company Eli Lilly, had received a conditional marketing authorisation, subject to further clinical trial results.

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