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Showing 2761–2770 of 32475 articles for “Art. R 623-17”
I.-The holder of the "A" authorisation pursuant to Article R. 6123-135 shall have a team comprising: 1° At least one doctor specialising in nuclear medicine present on site during patient care; 2° At…
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.
The provisions of paragraph 1 of sub-section 9, with the exception of those of II of article D. 6124-131, are applicable to the holder of a nuclear medicine qualification with grade B when carrying ou…
Staff working in the delimited area where radiopharmaceutical preparations and controls are carried out receive appropriate initial and ongoing training in radiopharmacy and radiation protection for s…
When a member of the Commission for the Protection of Access to Works has been contacted by a person directly or indirectly interested in a transaction submitted for its assessment, with the clear aim…
The right to object provided for in article 38 of amended law no. 78-17 of 6 January 1978 relating to information technology, files and freedoms does not apply to the processing referred to in article…
Amendment registration requests relating to a lien or pledge referred to in I. of Article R. 521-9 are also made at the Institut national de la propriété industrielle in the registers determined in II…
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