Article R5121-9-5
With a view to their inclusion in the register of hybrid groups mentioned in the last paragraph of Article L. 5121-10, hybrid medicinal products are identified by a decision of the Director General of…
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Showing 8101–8110 of 46083 articles for “Art. L 54-10-5”
With a view to their inclusion in the register of hybrid groups mentioned in the last paragraph of Article L. 5121-10, hybrid medicinal products are identified by a decision of the Director General of…
Articles 258 to 275 of Commission Delegated Regulation (EU) No 2015/35 of 10 October 2014 are applicable at group level.
For the application of 2° of I of Article L. 561-5, and by way of derogation from Article R. 561-5-2, when the measures provided for in 1° to 3° of Article R. 561-5-1 cannot be implemented: 1° The per…
Elected members of a Council of the Order who are not entitled to the allowance provided for in article D. 4311-55-1 may, in cases determined by the National Council, receive an allowance for particip…
The genetic counsellor may, in the cases defined by the organisational protocol provided for in Article R. 1132-5-2: 1° Prescribe the medical biology examinations mentioned in Article R. 1131-2 and in…
In the event of difficulties in the application, within an approved service, of the provisions of articles R. 6153-2 to R. 6153-2-3, R. 6153-10 and D. 6153-10-1, the representatives of students in the…
I. - The agreements provided for in article L. 132-28 are not required if the intermediary only uses advertising documents provided by the insurance company and the latter has undertaken in writing to…
Nature of the assignment carried out Amount of the flat-rate indemnity per assignment (expressed in units of value) Amount natural persons Amount associations To proceed with the reminder of the oblig…
I.-In application of 7° of article L. 5125-1-1 A, the patient may designate a pharmacist who holds a dispensary or who manages a mutualist or miner's aid pharmacy, participating in the same coordinate…
The importing pharmaceutical establishment shall ensure that the investigational medicinal products it imports have been subjected to standards of good manufacturing practice at least equivalent to th…
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