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Showing 7351–7360 of 66662 articles for “Art. 1251 and 1251-1”
Without prejudice to the information required by other legislative and regulatory provisions, the labelling of the outer packaging or, where there is no outer packaging, the labelling of the immediate…
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…
…ompatible with the summary of product characteristics. This information must be useful for patients and must not be promotional in nature. II -When the medicinal product or product has effects on the…
…h 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 to in articl…
…he purposes of this chapter, the following definitions shall apply 1° "Adverse reaction": a noxious and unintended response to a medicinal product or to a product mentioned in Article R. 5121-150 ; 2°…
…l product or a product mentioned in article R. 5121-150, including cases of overdose, misuse, abuse and medicinal errors as defined in article R. 5121-152, as well as the monitoring of adverse reactio…
…a postgraduate diploma attesting to studies relating to the activities concerned, when this diploma and the title of the training course appear on a list drawn up by order of the ministers responsible…
The head pharmacist 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 on…
The pharmacist in charge and the interim pharmacist in charge of the companies or organisations mentioned in 4°, 5°, 6°, 7°, 8°, 10°, 11°, 12°, 13°, 14° and 15° of article R. 5124-2 provide proof of a…
All pharmaceutical acts are carried out under the effective control of a pharmacist who meets the conditions for practising pharmacy in France.
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