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Showing 8411–8420 of 50062 articles for “Art. s. R 622-8 to R 622-9”
Advanced therapy medicinal products prepared on an ad hoc basis are distributed, under the responsibility of the person in charge referred to in article R. 4211-37 or, where applicable, the person in…
An authorised establishment or organisation may transfer to another authorised establishment or organisation advanced therapy medicinal products prepared on an ad hoc basis with a view to their storag…
Changes other than those mentioned in articles R. 4211-43 and R. 4211-44 are declared in the annual activity report provided for in article R. 4211-47.
In the event of non-compliance with the legislative and regulatory provisions or the conditions of the authorisation, the suspension, which may not exceed one year, and the withdrawal of the authorisa…
The authorised establishment or body sends the Director General of the Agence nationale de sécurité du médicament et des produits de santé and the Director General of the Agence de la biomédecine, as…
Any transfer or acquisition of radioactive sources is subject to prior registration with the Institut de Radioprotection et de Sûreté Nucléaire, using a form issued by this body, except in the cases d…
All imports or exports of radioactive sources from or to non-EU countries must be registered in advance with the Institut de Radioprotection et de Sûreté Nucléaire.The exporter or importer completes a…
I.-It is forbidden1° To transfer, whether temporarily or permanently, electrical equipment emitting ionising radiation, accelerators and radioactive sources, whether in return for payment or free of c…
I.- Pursuant to articles L. 1333-5, L. 1333-15 and L. 1333-16, this section defines, in particular, the conditions under which radioactive sources, electrical equipment emitting ionising radiation and…
The declaration provided for in Article 4 of Council Regulation (EEC) No 1493/93 of 8 June 1993 on shipments of radioactive substances between Member States shall be deposited with the Institut de Rad…
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