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Showing 1661–1670 of 4847 articles for “Art. 17 sept. 2020”
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 role of the radiopharmacist provided for in article D. 6124-189 is to ensure the safety of the radiopharmaceutical medicine circuit and includes in particular: 1° Carrying out control actions rela…
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…
…the exemption is subject to compliance with Article 14 of Commission Regulation (EU) No 651/2014 of 17 June 2014 declaring certain categories of aid compatible with the internal market in application…
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