Article D412-10
The duties of the person in charge of missions falling within the remit of the national plant variety authority are:receiving, registering and examining applications for plant variety certificates and…
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Showing 1041–1050 of 64732 articles for “Art. I-1°-d”
The duties of the person in charge of missions falling within the remit of the national plant variety authority are:receiving, registering and examining applications for plant variety certificates and…
An acknowledgement of delivery of the loaned item is issued by the caisse to the borrower at the same time as the borrower receives payment of the amount loaned. This acknowledgement is either issued…
In the event of loss of the acknowledgement of deposit of a pledged item, the borrower must immediately inform the institution. The institution shall record this loss in the deed referred to in II of…
Continuous monitoring is carried out in health establishments comprising one or, exceptionally, several units, if the size of the establishment justifies it, organised to care for patients who, due to…
The continuous surveillance unit may operate in a health care establishment that has neither a resuscitation unit nor an intensive care unit if it has signed an agreement specifying the conditions for…
I.-The holder of a "B" nuclear medicine authorisation pursuant to Article R. 6123-135 has an in-house pharmacy authorised to carry out the activity provided for in 6° of Article R. 5126-9 and, where a…
The equipment on the site authorised under the conditions of Article R. 6123-136 is connected to a system for archiving and sharing images and to a system for archiving and analysing doses. The report…
The authorised nuclear medicine site has the following equipment: 1° An emergency trolley for the treatment of patients requiring it; 2° Equipment for waste and effluent management in accordance with…
The authorisation holder is subject to the obligation of quality assurance defined in I of Article L. 1333-19.
Where the site has an in-house pharmacy, the preparation of radiopharmaceuticals must be carried out under its supervision.
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