Article R5127-23
After checking the integrity of the seals, the two experts are given the sample previously held by the owner or holder and the sample previously held by the agent who took the sample and forwarded to…
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Showing 921–930 of 2859 articles for “Art. 23 févr. 1994”
After checking the integrity of the seals, the two experts are given the sample previously held by the owner or holder and the sample previously held by the agent who took the sample and forwarded to…
The conditions under which List I and List II medicinal products are prescribed, held or distributed may, on public health grounds, be made subject, in whole or in part, to the provisions of sub-secti…
No container or packaging that has been in contact with micro-organisms and toxins or products containing them mentioned in article L. 5139-1 may receive products intended for human or animal consumpt…
I. - For the application of 1° of article R. 5141-18 , when reference is made to published scientific literature, the experts shall justify the use of this bibliographical documentation and demonstrat…
A pharmacist or veterinary surgeon providing a replacement must register for this purpose with the order to which he belongs and register his diploma, under the conditions provided for in article L. 4…
In order to comply with the essential requirements relating to design and manufacture, active implantable medical devices must be designed, manufactured and packaged in such a way as to meet the follo…
As part of the procedure applicable to in vitro diagnostic medical devices undergoing an assessment of their performance, the manufacturer must draw up a declaration containing the data enabling the d…
Manufacturers of medical devices and the companies and organisations operating these devices shall, at the reasoned request of the Director of the Agence nationale de sécurité du médicament et des pro…
Failure to comply with the provisions of the third paragraph of Article L. 6144-1 and the fourth paragraph of Article L. 6161-2 may be recorded by the Director General of the Regional Health Agency, p…
The authorisation holder shall carry out the assessment referred to in Article L. 6122-5, in accordance with the conditions laid down in this section.The purpose of this evaluation is to check that th…
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