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Showing 3911–3920 of 57397 articles for “Art. L. 611-4 to L. 611-16”
The doctor, dental surgeon, midwife, pharmacist or nurse shall immediately report any adverse reaction suspected of being due to a medicinal product or to a product mentioned in article R. 5121-150 of…
For reasons relating to the protection of public health, the measures provided for in article R. 5122-15 may be taken in the event of misuse, as defined in article R. 5121-153, or drug dependence or a…
A private practice company may not operate more than one pharmacy.
When applying for registration, the ministries and certifying bodies inform the Director General of France Compétences of the authorisations they have issued to bodies to prepare for the acquisition,…
…a savings passbook instituted by article 80 of law no. 76-1232 of 29 December 1976 who are planning to set up or acquire a craft business, as well as their spouse, partner in a civil solidarity pact o…
I.-The user, provider of actions contributing to the development of skills, enters, records and transmits the data mentioned in article R. 6351-15. II.-The user, an agent responsible for monitoring vo…
The results of the analyses and the conclusions of the analysis report are communicated to the officials who drew up the report or the sampling record and, as appropriate, to the Agence nationale de s…
The authorisation holder shall inform the Director General of the Agency of the commencement of the activity covered by the authorisation. He shall also inform him of the definitive cessation of this…
…rian(s) must have at least two years' practical experience in one or more establishments authorised to manufacture or import veterinary medicinal products in a Member State of the European Community o…
At the request of the Director General of the Agence nationale de sécurité du médicament et des produits de santé, the manufacturer or its authorised representative shall provide any information relat…
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