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Showing 4991–5000 of 58742 articles for “Art. s. 1844-11 and 1844-13”
In blood transfusion establishments and in any organisation other than pharmacies, health establishments and health cooperation groups authorised to dispense blood-derived medicinal products, these me…
…g, known as traceability, from the time they are manufactured until they are administered to patients. The purpose of this monitoring is, in particular, to enable rapid identification of : 1° The bloo…
In healthcare establishments and other establishments with an in-house pharmacy, blood-derived medicinal products are dispensed by the in-house pharmacy on the basis of a medical prescription.The in-h…
…immediately transcribe the information mentioned in article R. 5132-10, the patient's date of birth and the information appearing on the detachable label of the outer packaging onto a special register…
…medicinal products must, when disposing of these medicinal products, record :1° The name, strength and pharmaceutical form of the medicinal product concerned ;2° The batch number and the number of un…
I.-The protocol is drawn up, monitored and developed by a steering committee, co-chaired by a representative of the Minister for Defence and a representative of the Minister for Health. The committee…
I.-The protocol referred to in I of article L. 6147-11 is implemented for a period of five years and tacitly renewed for the same period, unless an amendment is concluded no later than six months befo…
I.-In exceptional circumstances, when collective and individual protection measures are unable to guarantee that workers' exposure remains below the exposure limit values provided for in Article R. 44…
The employer shall ensure that the worker concerned: 1° Has given his agreement to carry out this work; 2° Has the benefit of all the appropriate means of protection; 3° Is classified as category A; 4…
…secutive years, including the years in which the limit was exceeded, does not exceed 20 millisieverts.
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