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Showing 4611–4620 of 38200 articles for “Art. R. 210-6”
The members of the Medical Risks Observatory mentioned in 5° to 12° of article D. 1142-59 are appointed by order of the ministers responsible for health, social security and the economy for a renewabl…
The Medical Risks Observatory may only deliberate if at least half of its members in office, including the Chairman or, in his absence, the Vice-Chairman, are present. Decisions are taken by a majorit…
…g) The nature and results of tests and analyses meeting the requirements of section 2 of this chapter. The nature and results of the tests and analyses must be certified by the natural or legal person…
The authorisation to import labile blood products for direct therapeutic use is issued by the Agence nationale de sécurité du médicament et des produits de santé to the Armed Forces Blood Transfusion…
…t all the results of the tests and analyses comply with the requirements of section 2 of this chapter.
When the import concerns plasma pastes or labile blood products intended for the preparation of health products, the authorisation referred to in Article D. 1221-58 is issued to the following organisa…
…du médicament et des produits de santé on the basis of a forward programme submitted by the importer. At the end of the authorisation period, the importer draws up a report on the operations carried…
…rt authorisation is requested was prepared, comply with the requirements of Section 2 of this chapter. Where this is not the case, and provided that it is justified, the importer must provide an under…
…mponents from which this product has been prepared meet the requirements of section 2 of this chapter.
The importer is required to: 1° Ensure that the establishment that collected or took the sample undertakes to pass on any information that could call into question the quality and safety of the produc…
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