Article R5121-107-6
…n or a combination thereof included in the list drawn up for use in traditional herbal medicinal products by the Commission of the European Communities pursuant to Article 16f of Directive 2001/83/EC…
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Showing 6401–6410 of 34927 articles for “Art. Aut. conc. n° 22-D-10 du 12 Apr 2022”
…n or a combination thereof included in the list drawn up for use in traditional herbal medicinal products by the Commission of the European Communities pursuant to Article 16f of Directive 2001/83/EC…
If, after a traditional herbal medicinal product has been registered, the proprietor considers, on the basis of new data available to him, that, given its characteristics, the medicinal product is now…
…by the Commission of the European Communities, any registration of traditional herbal medicinal products containing this substance is cancelled by the Director General of the Agency, unless the holde…
I.-The period of traditional medical use provided for in 4° of Article L. 5121-14-1 is thirty years, including at least fifteen years in a Member State of the European Community or in another State pa…
I.-The registration of the medicinal products mentioned in article L. 5121-13 may be refused, amended, suspended or withdrawn by the Director General of the Agency. The period of suspension may not ex…
Where the application for registration concerns a product which has been the subject of a Community herbal monograph established by the Committee for Herbal Medicinal Products of the European Medicine…
Non-compliance with the provisions governing the formation and operation of sociétés de participations financières de profession libérale de pharmaciens d'officine by pharmacists who are members of su…
Tattoo products are subject to vigilance designed to monitor undesirable effects occurring under normal conditions of use of the product or resulting from misuse. This vigilance is applied to all thes…
Tattoo products are rendered sterile using appropriate processes. They are supplied in a container which retains sterility until use. Multiple dose containers are authorised provided that the delivery…
…ty or be associated with a holder of this authorisation under the conditions set out in article R. 6123-90-1. A protocol for the patient's care pathway undergoing systemic cancer drug treatment is dra…
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