Article R5334-1
Failure to comply with the provisions of articles L. 5331-1, L. 5331-2, L. 5331-4, L. 5332-1 and L. 5332-3, relating to the conditions for publication and dissemination of job offers, is punishable by…
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Showing 7311–7320 of 59417 articles for “Art. Cass. 3e Civ. 8-1-1997 n° 9”
Failure to comply with the provisions of articles L. 5331-1, L. 5331-2, L. 5331-4, L. 5332-1 and L. 5332-3, relating to the conditions for publication and dissemination of job offers, is punishable by…
The authorisation holder must ensure that a radiotherapist with the qualifications listed in Article D. 6124-133 and a medical physicist are present on the authorised site throughout the period of tre…
Outside the operating hours of the radiotherapy unit and by way of derogation from article D. 6124-133-2, the holder of the brachytherapy authorisation practising brachytherapy continuously over more…
The holder of the radiotherapy or brachytherapy authorisation makes the necessary arrangements with the professionals concerned for : 1° The final validation of the delineation of target volumes and o…
The licence holder practising radiotherapy in stereotactic conditions has the appropriate technique for monitoring anatomical structures in real time and for acquiring anatomical data with a view to p…
Where the licensee has a particle accelerator with on-board magnetic resonance imaging equipment, it has a pre-established protocol drawn up by the radiotherapy team, involving qualified doctors speci…
The authorisation holder ensures that each patient's external radiotherapy treatment is carried out by two medical radiation technologists present at the treatment station in the radiotherapy unit.
Pursuant to article L. 6145-16, the accounts of public health institutions may be certified by one or more statutory auditors or, for institutions whose total income from the main profit and loss acco…
A medicinal product or a series of medicinal products mentioned in Article L. 5121-13 may only be registered if the applicant is established in a Member State of the European Community or a party to t…
…peutic effect being required, and defining the degree of dilution above which safety is guaranteed; 9° For each pharmaceutical form, a document relating to the manufacture and control of the medicinal…
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