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Showing 3531–3540 of 61711 articles for “Art. R 330-2 · Cass. com. 7 July 2004 · CA Paris 5 November 2008”
The manufacturer undertakes to fulfil all the conditions necessary for the approved quality system to remain effective.
The notified body checks, by means of surveillance, that the manufacturer duly fulfils the obligations arising out of the approved quality assurance system.
The manufacturer must allow the notified body access to the locations of design, manufacture, inspection, testing and storage and must provide all necessary information, in particular: 1° the document…
If the body considers that the conditions necessary for approval of the quality system are no longer fulfilled, it will withdraw this approval. This withdrawal prohibits the placing on the market of t…
The notified body carries out periodic audits to ensure that the manufacturer maintains and applies the approved quality system. It provides the manufacturer with an audit report. The frequency of the…
The reference headcount is the average headcount for the calendar year preceding the year in which approval is granted. It is calculated in accordance with article L. 1111-2 and rounded to the nearest…
The Conseil national d'orientation des conditions de travail : 1° Participates in the preparation of national and international strategic guidelines relating to health and safety at work, the improvem…
In the case of training courses involving a distance from the trainee's usual place of residence, the trainees concerned are entitled, in order to enable them to return periodically, to reimbursement…
The provisions of Article R. 332-16 apply to the insurance undertakings referred to in Article L. 310-3-1.
I.-When the holder of an external radiotherapy authorisation carries out treatments using the proton therapy technique, he also has an authorisation on the same site to hold heavy cyclotron equipment…
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