Article R5142-22
A pharmacist or veterinary surgeon in charge or delegate registers with the order to which he belongs, and registers his diploma, under the conditions provided for in article L. 4221-16 for pharmacist…
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Showing 4631–4640 of 53874 articles for “Art. R 110-2”
A pharmacist or veterinary surgeon in charge or delegate registers with the order to which he belongs, and registers his diploma, under the conditions provided for in article L. 4221-16 for pharmacist…
In carrying out certification procedures, manufacturers and approved bodies shall take account of the available results of any assessment and verification operations which may have been carried out, p…
The manufacturer or his authorised representative shall, for a period of at least five years and, in the case of implantable devices, at least fifteen years after the last copy of the product has been…
For the purposes of article L. 5143-3, a user approved to carry out the extemporaneous preparation of medicated feedingstuffs means the professional keeper of animals belonging to species whose flesh…
Medical devices intended for the administration of a medicinal product are governed by this Title.However, where a device forms with a medicinal product an integrated product intended exclusively for…
Files and correspondence relating to certification procedures are drawn up in French or in a language of a Member State of the European Union or party to the Agreement on the European Economic Area ac…
The labelling of a medical device given to the end user or patient, the accompanying leaflet and any other information relating to its operation or use must include a version written in French.
The conditions for implementing the essential requirements defined in this section are specified, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produ…
Where the conformity certification procedure applied by a manufacturer involves the intervention of an authorized body, the manufacturer may apply to the body of his choice within the framework of the…
As part of the EC verification procedure, the manufacturer shall submit to an authorized body for inspection devices manufactured in conformity with an approved type as described in an EC type-examina…
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