Sentence examples for authorisation was issued from inspiring English sources

The US says a last-minute authorisation was issued late on Thursday for the request lodged a day earlier, rather than the three days' notice required.

For example, guidance on the use of vinorelbine for advanced breast cancer (TA 54) 10 was published in 2002, whereas its marketing authorisation was issued in 1997, 2 years before NICE existed.

The Home Office said that in most of the cases authorisations were issued for periods beyond the 28-day statutory limit for each operation or were not signed off by ministers within the statutory 48-hour deadline.

The vice-chair of the Australian Privacy Foundation, David Vaile, has called into question the effectiveness of these safeguards because the authorisations are issued by the defence minister and not a judge.

A licence to crenellate - a form of royal authorisation for a new castle - was issued by Edward II in 1316, and a castle constable was appointed in 1319, charged with defending both the castle and the surrounding manors of Embleton and Stamford.

Recently in the EU, a new regulation was issued for enzymes under Regulation (EC) No. 1332/2008 and a new authorisation procedure under Regulation (EC) No. 1331/2008 was adopted (as discussed above).

Recently in the EU, a new regulation was issued for flavouring substances under Regulation (EC) No. 1334/2008 and a new authorisation procedure under Regulation (EC) No. 1331/2008 was adopted (as discussed above in "Direct food additives").

"If they do so without the school's authorisation they are issued with a fixed penalty, but where the penalty is not paid it may result in court action," he said.

Sertraline use in this context is acceptable, but patients should be advised about the evidence for its use and warned that no marketing authorisation (licence) has been issued for the drug's use in generalised anxiety disorder.

The majority of these recalls were issued by the manufacturers or marketing authorisation holders using the Health Product Recall type I, II and III, which accounted for 95% of the total substandard medicines reported.

This means that authorisation of the most intrusive investigatory powers, whereby intercept warrants are issued by the secretary of state, will not come into force until formally approved by a judge.