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Showing 1091–1100 of 3486 articles for “Art. 20 Oct 2011”
Before administering the punctually prepared advanced therapy medicinal product, the health professional in the health establishment must ensure that the information required for the traceability of t…
The pharmacovigilance carried out on individually prepared advanced therapy medicinal products includes monitoring to ensure traceability between the various stages, from the removal of tissues, cells…
I.-Any establishment or body referred to in Article L. 4211-9-1 or any pharmaceutical establishment referred to in Articles L. 5124-1 or L. 5124-9-1 shall set up and keep up to date a system ensuring…
In the event of interruption or cessation of activity of an establishment or organisation mentioned in article L. 4211-9-1, the data relating to the traceability of advanced therapy medicinal products…
The data referred to in II and III of Article R. 5121-201-5 and a copy of the administration record referred to in Article R. 5121-201-6 shall be kept by the establishments referred to in Article R. 5…
I.-The members of the Board of Directors must be in active employment or have been in active employment during the five years preceding their appointment. They may be represented by an alternate appoi…
The regional inter-professional joint committee is responsible for: 1° Examining, authorising and paying for the professional transition projects provided for in article L. 6323-17-2 and the professio…
I.-The board of directors of the regional joint cross-industry committee is composed, taking into account the representativeness of the signatories of the agreement establishing the committee, of no m…
The regional cross-industry joint committees manage the funds received to finance professional transition projects in application of 5° of article L. 6123-5 within two separate financial sections: 1°…
The provisions of articles R. 6332-13, R. 6332-14 and R. 6332-34 to R. 6332-37 are applicable to the regional joint cross-industry committees.
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