Article R5132-78
…des produits de santé. This authorisation is issued under the conditions set out in article R. 5132-75. The authorisation mentions the name and quantity of the product involved in the operation, the n…
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Showing 3861–3870 of 12170 articles for “Art. 7 Jan 1987”
…des produits de santé. This authorisation is issued under the conditions set out in article R. 5132-75. The authorisation mentions the name and quantity of the product involved in the operation, the n…
The report or record : 1° Contains a brief description of the circumstances in which the sample was taken ; 2° Relates : a) The marks and labels affixed to the primary or outer packaging ; b) The size…
The authorisation referred to in article R. 5132-74 may only be granted to a natural person. In the companies mentioned in articles L. 5124-2 and L. 5142-1, authorisation may be requested for the phar…
…to in the first paragraph is granted or withdrawn under the conditions set out in Articles R. 5132-75 to R. 5132-77. The authorisation is also subject to the holder of the authorisation recording the…
Doctors, veterinary surgeons and the groups defined in article L. 5143-6 who are authorised to supply medicinal products are subject to the obligations imposed on pharmacists by this chapter, subject,…
For the purposes of this section, : "Misuse" means use which does not comply with the intended purpose of the product, its normal or reasonably foreseeable use or its instructions for use, or with the…
The authorisation provided for in Article R. 5132-74 is issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé, after obtaining the opinion of the Di…
Containers or packaging containing narcotics and used for their import or export, transport or possession must bear a label of a size appropriate to their volume, affixed in such a way that it cannot…
Active substances may only be imported for the manufacture of medicinal products for human use from a third country into the European Union if they are accompanied by written confirmation from the com…
When the application for authorisation concerns all or part of the micro-organisms or toxins or products containing them, intended for veterinary use, the Director General of the Agence nationale de s…
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