Article R5141-123-8
I. - The veterinary medicinal product for which parallel import authorisation is requested may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provid…
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Showing 4231–4240 of 49599 articles for “Art. 25-8 I”
I. - The veterinary medicinal product for which parallel import authorisation is requested may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provid…
If the ministerial authority does not respond to an application submitted under articles L. 4131-4 and L. 4131-4-1 within four months of receipt of a complete application, this will be deemed to const…
In the absence of a stipulation in the agreement or branch agreement concluded in application ofarticle L. 1242-8, the total duration of the fixed-term employment contract may not exceed eighteen mont…
For the application of the second and third paragraphs of Article L. 621-2, the matter shall be referred to the court by means of a writ of summons for the purpose of extending the proceedings or reun…
I.-The pharmacist working in a dispensary, a mutualist pharmacy or a dispensing chemist may prescribe and administer the vaccines mentioned in the decrees provided for respectively by 9° and 9° bis of…
The use of health data and administrative data referenced with the national health identifier is only authorised as part of personal data processing if the following two conditions are met:1° The purp…
The national health identifier is used to reference the health data and administrative data of any person receiving or due to receive a diagnostic, therapeutic, preventive, pain-relieving, disability-…
The Public Prosecutor at the Paris Court of Appeal grants or refuses authorisation by decree. Where he is considering refusing authorisation, he shall inform the interested party, specifying that he m…
Decisions to include a medicinal product in the register of hybrid groups, to amend these decisions and to remove a medicinal product from this register, governed by this section, are published on the…
The cost of monitoring treated patients is borne by the marketing authorisation holder for the medicinal product or by the company which operates the medicinal product and which has been authorised to…
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