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Showing 9231–9240 of 67137 articles for “Art. L. 145-11 + Art. R. 145-1”
…ducts and for products which must be covered by the marketing authorisation provided for in article L. 5121-8, after this authorisation has been issued;2° For the medicinal products mentioned in artic…
When registration is suspended or withdrawn, the holder informs the stockholders without delay. They must take all necessary steps to stop the distribution of the medicinal product. If these steps are…
Registration of homeopathic medicinal products and traditional herbal medicinal products, as well as suspension and withdrawal of registration, are made available to the public by the Director General…
…comply with the information given in the summary of product characteristics referred to in article R. 5121-21 and with the therapeutic strategies recommended by the Haute Autorité de santé referred t…
…ion": a noxious and unintended response to a medicinal product or to a product mentioned in Article R. 5121-150 ; 2° "Serious adverse reaction": an adverse reaction which is lethal or life-threatening…
…g of adverse reactions suspected to be due to a medicinal product or a product mentioned in article R. 5121-150, including cases of overdose, misuse, abuse and medicinal errors as defined in article R…
The duration of the practical experience provided for in article R. 5124-16 is reduced to one year for pharmacists whose studies were carried out under a five-year system. It is reduced to six months…
…and the delegate pharmacist(s) of the companies or organisations mentioned in 1° and 2° of article R. 5124-2 must provide evidence of at least two years' practical experience in one or more establish…
All pharmaceutical acts are carried out under the effective control of a pharmacist who meets the conditions for practising pharmacy in France.
…t submits each group or company agreement implementing the employment obligation set out in article L. 5212-2 to:1° The regional coordination committee for employment and vocational training in the ov…
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