Traduction de «Période de pré-enregistrement » (Français → Anglais) :

canned audio-visual material

pre-bidding | pre-bidding phase

taped commentary [ tape commentary | taped presentation | tape-recorded narration | tape-recorded commentary | recorded sound commentary ]

Production and Sales of Phonograph Records and Pre-Recorded Tapes in Canada

With the financial support of the Commission and support on the ground from the European Asylum Support Office (EASO) and the United Nations High Commissioner for Refugees (UNHCR), the Greek asylum service launched a major pre-registration exercise on 8 June with the aim to pre-register 1,400 persons per day to accelerate the identification and full processing of relocation applicants.

Greece is preparing a major pre-registration exercise that will accelerate the identification and full registration of relocation applicants.

(13)cybersquattingtop-level domainSunrise PeriodPricewaterhouseCoopersEURid The sunrise period of domain registration is a special period during which trademark holders may preregister names that are the same or similar to their trademarks in order to avoid .

With reference to the antimalarial drug mefloquine administered to Canadian Forces bound for Somalia in 1992-93 and the legal framework under which it was available for use and administered: (a) was mefloquine a licensed drug when it was administered to Canadian Forces, if not what was its status, and how was it legally available; (b) were the Canadian Forces participating in the Lariam (mefloquine) Safety Monitoring Study during this period; (c) was the mefloquine administered in accordance with the Lariam Safety Monitoring Study and the Food and Drug Act; (d) who was the “principal investigator” responsible for the Lariam Safety Mon ...[+++]itoring Study in the Canadian Forces; (e) who was the Canadian Forces physician responsible to the “principal investigator” of the Lariam Safety Monitoring Study; (f) what was the role of Canadian Forces physician, Dr. Martin Tepper, in the Lariam Safety Monitoring Study; (g) who was responsible for the Lariam Safety Monitoring Study at the Department of Health's Health Protection Branch during this period; (h) what was the role and responsibility of the Health Protection Branch under the Lariam Safety Monitoring Study and the Food and Drug Act and its regulations in regard to the use of mefloquine by Canadian Forces personnel; (i) when did the Health Protection Branch become aware that mefloquine was being administered to Canadian Forces personnel bound for Somalia; (j) what responsibility did the Canadian Forces have under the Lariam Safety Monitoring Study and the Food and Drug Act prior to the licensing of mefloquine to inform the manufacturer of its use; (k) what responsibility did the Canadian Forces have under the Lariam Safety Monitoring Study and the Food and Drug Act to the soldiers who were administered the drug; (l) did the Canadian Forces fulfil their responsibility to the manufacturer under the Lariam Safety Monitoring Study and the Food and Drug Act prior to the licensing of mefloquine and if so how did they do ...