Article R1333-108
The provisions of this sub-section define the declaration procedures required, pursuant to article L. 1333-8, for the nuclear activities mentioned in articles R. 1333-109 and R. 1333-110.
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Showing 4811–4820 of 68192 articles for “Art. s. R 232-22 and R 123-154-1”
The provisions of this sub-section define the declaration procedures required, pursuant to article L. 1333-8, for the nuclear activities mentioned in articles R. 1333-109 and R. 1333-110.
The rates and conditions for awarding the fixed allowances provided for in articles R. 2523-17 and R. 2523-18 and the holiday allowances are set by joint order of the ministers responsible for labour,…
The provisions of articles R. 4331-12 to R. 4331-15 are applicable to the provision of services by speech and language therapists whose declaration is required under article L. 4341-7.
Authorisations to set up, transfer or group pharmacies are subject to compliance with the conditions set out in articles R. 5125-8 and R. 5125-9 and in 2° of article L. 5125-3-2.
The provisions relating to professional secrecy, set out in the last paragraph of article R. 6251-2, are applicable to the experts appointed by the consular chambers mentioned in article R. 6261-16.
The authorisation holder shall record any acquisition, transfer, import or export of micro-organisms and toxins or products containing them in a special register or by any appropriate computer system.…
The authorisation is issued to the natural or legal person responsible for the nuclear activity and is not transferable. It may impose appropriate restrictions on the conditions under which the nuclea…
Any medicinal product which does not have a marketing authorisation as referred to in Article L. 5121-8 or an early access authorisation as referred to in Article L. 5121-12 or a compassionate access…
The employer informs the trade union organisations representing employees in the company or in the establishment(s) concerned, of the completion of the prior declaration formalities with the Commissio…
The sponsor provides clinical trial investigators with : 1° The title and objective of the trial requested; 2° The pharmaceutical form, batch number(s) and expiry date of the investigational medicinal…
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