Article D6124-172
…or have carried out twenty-four hours a day, within a timeframe compatible with safety requirements and the patient's condition: - haematology, biochemistry and bacteriology tests ; - histocompatibili…
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Showing 2191–2200 of 66740 articles for “Art. 1873-1 and 1873-13”
…or have carried out twenty-four hours a day, within a timeframe compatible with safety requirements and the patient's condition: - haematology, biochemistry and bacteriology tests ; - histocompatibili…
…ises on-site or on-call medical care to ensure that haematopoietic cell transplants are carried out and that continuity of care is maintained at all times.
The operating theatre is adapted to the conditions of cell harvesting and the radiotherapy resources mentioned in article D. 6124-172 are adapted to whole body irradiation in paediatrics.
…with at least two years' training in a unit providing haematopoietic cell transplants. The nursing and paramedical staff are experienced in caring for children undergoing transplants and include at l…
…external valuation experts referred to in article L. 214-24-15 to comply with the laws, regulations and professional obligations applicable to them is subject to sanctions imposed by the Enforcement C…
I. - Electronic money issuers referred to in 1°, 1° ter and 1° quater of Article L. 561-2 may defer verification of the identity of their customer and, where applicable, of the customer's beneficial o…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé: 1° Records any adverse reaction suspected to be due to a medicinal product or to a product mentioned in…
…é du médicament et des produits de santé shall fulfil its obligations in terms of pharmacovigilance and participation in European Union activities in this field.The National Agency for the Safety of M…
…cy may ask the regional pharmacovigilance centres to carry out any pharmacovigilance investigations and work.He may also ask the drug dependence and addictovigilance assessment and information centres…
…d in II to IV of this article. II.It informs the European Commission, the European Medicines Agency and the other Member States of the European Union of one of the following situations: 1° It is consi…
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