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Showing 4621–4630 of 59015 articles for “Art. 10 and 11”
…of decree no. 2008-436 of 6 May 2008 relating to the registration of homeopathic medicinal products and traditional herbal medicinal products, the period is counted from this date. However, the Direct…
…registration dossier. This information concerns in particular the assessment of the quality, safety and homeopathic use of the medicinal product in the case of homeopathic medicinal products, the risk…
After registration, manufacturing methods and control techniques take account of scientific and technical progress. Any resulting changes must first be registered under the conditions set out in artic…
A medicinal product or a series of medicinal products mentioned in Article L. 5121-13 may only be registered if the applicant is established in a Member State of the European Community or a party to t…
…the Agency will take all appropriate measures. Independently of suspension or withdrawal decisions and for the reasons that justify them, the Director General of the Agency may prohibit, as a precaut…
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…
…er I of this title, it may only be advertised to prescribers authorised to draw up the prescription and to pharmacists practising in establishments capable of dispensing the medicinal product.
…fer or group pharmacies are subject to compliance with the conditions set out in articles R. 5125-8 and R. 5125-9 and in 2° of article L. 5125-3-2.
I.-In order to enable apprentices to complete their training, in application of article L. 6221-1, part of their practical training may be provided in companies other than the one employing them, in p…
…part of a professional transition project to his employer in writing, no later than: 1° One hundred and twenty days before the start of the training course when the completion of the course entails a…
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