The phrase "authorisation date" is correct and usable in written English.
It can be used to refer to the specific date on which authorization was granted or approved for a particular action or document.
Example: "Please ensure that all documents are submitted before the authorisation date to avoid any delays."
Alternatives: "approval date" or "authorization timestamp".
The current authorisation dates back to 2001, is narrowly tied to the September 11th attacks and gives the president sweeping powers.
10 11 12 13 Research on repeat prescribing has been largely quantitative, comprising retrospective surveys of conditions, drugs, authorisation dates, clinicians' views, 2 14 15 16 17 and experimental or quasi-experimental studies of interventions aimed at improving efficiency or safety.
5 This period was further subdivided by the date of Marketing Authorisation Application (MAA, regulatory submission or 'filing') into periods representing clinical trials (prior to filing) and subsequent regulatory approval.
Table 1 summarises when the products were originally licensed, the date of the latest authorisation and the date of the most recent substantive change to the SPC.
To avoid potential bias due to time-related differences in the probability of getting authorisation, for each authorised product, a random sample of up to two designated products from the same time period (120 days before to 120 days after) as the designation date of the authorised product was selected.
He gave his authorisation for that in a document dated 30 June.
Treatment started on the quit date, in line with marketing authorisation of NRT in France.
"We handle the heavy lifting of data model mappings, authorisation flows and keeping it all up to date and working".
The authorisation requirement applies with effect of the sunset date stipulated in the specific Annex XIV entry, while in the case of the restriction according to Article 69(2) REACH ECHA starts to consider action only after such date.
For each product, the following information was abstracted: generic name, brand name, manufacturer, indication, date of notice of compliance (NOC marketing authorisation), type of review (priority or standard) and type of product (traditional or biological).
