Translation of "Mise en tas " (French → English) :

sand stacking

progressive burning | forced burning | swamper burning

commissioning engineer

fish canner | fish canning operative | fish canning operator

canning and bottling worker | canning operative | canner | canning and bottling line operator

sequestration

stacker-reclaimer

dolly block | dolly

on the job training bonus [ on-site training bonus ]

thick wedge dolly

The topics discussed at these seminars included the implementation of the arrangements for evaluation and monitoring and the performance reserve, the implementation of the single computer system to manage the SPDs, management and inspection systems, the procedure for implementing financial corrections, the content of the annual reports, the procedure for taking decisions on major projects, the introduction of global grants, implementation of the territorial aspects of the SPDs and the establishment and implementation of the communications plans.

If a medicinal product is authorised for a paediatric indication and the marketing authorisation holder has benefited from rewards or incentives under Article 36, 37 or 38, and these periods of protection have expired, and if the marketing authorisation holder intends to discontinue placing the medicinal product on the market, the marketing authorisation holder shall transfer the marketing authorisation or allow a third party, which has declared its intention to continue to place the medicinal product in question on the market, to use the pharmaceutical, pre-clinical and clinical documentation contained in the file of the medicinal produ ...[+++]ct on the basis of Article 10c of Directive 2001/83/EC.

Second assessment of progress made in implementing the Broad Economic Policy Guidelinesproviding input for the 2005 Spring Report | This Communication reviews progress made in implementing the EU’s medium-term economic policy strategy as set out in the 2003-05 Broad Economic Policy Guidelines (BEPGs).[1] Having been adopted in 2003 and updated in 2004[2] to take account of the Union’s enlargement, the guidelines focus on the contri ...[+++]bution that economic policies can make to the Lisbon strategy, both through the pursuit of sound macro-economic policies and vigorous economic reform.

In addition to the summary of the results, where the clinical trial was intended to be used for obtaining a marketing authorisation for the investigational medicinal product, the applicant for marketing authorisation shall submit to the EU database the clinical study report within 30 days after the day the marketing authorisation has been granted, the procedure for granting the marketing authorisation has been completed, or the applicant for marketing authorisation has withdrawn the application.