Article R1232-15
…he information required to ensure compliance with the legal and regulatory conditions for the samples.
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Showing 8861–8870 of 61869 articles for “Art. R. 512-39-1 et s.”
…he information required to ensure compliance with the legal and regulatory conditions for the samples.
…of the provisions of this chapter, army hospitals shall be deemed to be public health establishments. For these hospitals, the Minister for Defence exercises the powers of the Director General of the…
…mples in an establishment to make cell therapy preparations for therapeutic purposes, an agreement between the blood transfusion establishment and the health establishment lays down the conditions for…
…vity and operation of the automated national register of refusals to consent to the removal of organs.
The provisions of this chapter shall apply to army hospitals. For these hospitals, the Minister for Defence shall exercise the powers of the Director General of the Regional Health Agency.
Establishments authorised to carry out cell sampling take the necessary steps to ensure that all documents relating to the sampling are kept in accordance with the rules of good cell sampling practice…
Each year, the establishments authorised to carry out cell harvesting transmit to the director of the regional hospitalisation agency and to the director general of the Agence de la biomédecine the in…
Implementation of the protocol may begin on expiry of the two-month period following issue of the acknowledgement of receipt, unless the Minister responsible for research decides to prohibit implement…
For the application of the provisions of this chapter, army hospitals and the army blood transfusion centre shall be regarded as public health establishments and a blood transfusion establishment resp…
The Director General of the Agence de la biomédecine must be informed of any change in the information contained in the file during the implementation of the protocol. The latter will inform the Minis…
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