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Showing 91–100 of 37773 articles for “Art. L 1221-19”
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…
This section applies to plasma pastes and labile blood products intended for the preparation of health products. It also applies to labile blood products for direct therapeutic use included on the lis…
At the express request of the departments responsible for employment control, the employer shall provide the addresses of employees whose employment contracts have been concluded or terminated, as ref…
The body referred to in article R. 1221-3 shall keep the data contained therein for a period of six months from the date of receipt for the purposes of the administrations, departments, bodies or inst…
Blood or its components may only be used to prepare labile blood products intended for direct therapeutic use if the results of the screening tests provided for in 5° of article D. 1221-6 are negative…
…up, the Steering Committee: 1° Appoints a chairman from among the members sitting under 1° of Article R. 1221-23; 2° Draw up its own rules of procedure.
For each trainee referred to in the third paragraph of article L. 1221-13, the additional information, entered in the single personnel register or, for organisations that do not have a single personne…
Any blood establishment collecting blood and its components, which prepares labile blood products intended for the preparation of intermediate products or medicinal products derived from blood, is req…
Non-substantial modifications must be declared to the regional health agency. A copy is sent to the Etablissement français du sang or, where applicable, to the Centre de transfusion sanguine des armée…
With the exception of army pharmacists, pharmacists practising in health establishments, when they are responsible for supervising a blood depot mentioned in article R. 1221-20, must, for this activit…
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