Article D6124-133-7
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…
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Showing 4261–4270 of 61852 articles for “Art. Cass. 1re civ. 4 December 2013 · Cass. com. 15 November 2005 · Cass. com. 2 April 1974 · Cass. com. 13 May 1980”
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…
Any referral of a patient to another radiotherapy authorisation holder for cancer treatment by proton therapy is recorded in writing to ensure traceability.
…follow-up of the patient after treatment provided for in 3° and the fifth paragraph of article R. 6123-93 are recorded in the patient's medical record.
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.
…e authorisation holder is subject to the obligation of quality assurance defined in I of Article L. 1333-19.
…or by the civil party, the court shall rule in accordance with the penultimate paragraph of article 464. A judgment rendered in absentia, on the opposition of the accused, may be opposed under the con…
Manufacturers, importers and distributors of electric or electronic blood pressure monitors and thermometers shall ensure the availability of spare parts, in particular those listed as follows, for a…
Manufacturers, importers and distributors of sit-to-stand lifts shall ensure the availability of spare parts, in particular those listed as follows, for a minimum period of five years from the date on…
Manufacturers, importers and distributors of patient lifting equipment shall ensure the availability of spare parts, in particular those listed as follows, for a minimum period of five years from the…
The medical devices listed in this section are medical devices within the meaning of Article 2 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 concerning medi…
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