Article R1321-15
The health inspection referred to in 2° of I of article L. 1321-4 is carried out by the Regional Health Agency. It includes any operation to check compliance with legislative and regulatory provisions…
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Showing 421–430 of 32720 articles for “Art. R 623-15”
The health inspection referred to in 2° of I of article L. 1321-4 is carried out by the Regional Health Agency. It includes any operation to check compliance with legislative and regulatory provisions…
I. - direct or indirect holdings in the companies referred to in 2° of the I of article L. 214-115 may represent up to 100% of the assets of a société civile de placement immobilier, if the following…
The special purpose vehicle is managed by a manager appointed in accordance with the conditions laid down in its articles of association. When the special purpose vehicle is set up in a public scienti…
I. - For the purposes of this section, the following definitions apply- collective water misting systems: devices generating water aerosols, within establishments open to the public and places accessi…
Pharmacovigilance is carried out :1° For medicinal products and for products which must be covered by the marketing authorisation provided for in article L. 5121-8, after this authorisation has been i…
I.-Where the purpose of a cooperation grouping is to use the authorisations held by one or more of its members, the decision of the Director General of the Regional Health Agency provided for in Artic…
The guarantee fund may intervene, even before the criminal courts and even for the first time on appeal, with a view, in particular, to contesting the principle or the amount of the compensation claim…
Only the following personal data and information may be recorded in the processing provided for in article R. 332-14 the following personal data and information: 1° Identification data: surname; first…
The proposed formation of a European holding company is the subject, by each company registered in France that participates in the transaction, of a notice inserted in a medium authorised to receive l…
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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