Article R5132-7
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,…
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Showing 7511–7520 of 18871 articles for “Art. CA Douai 12-7-2018 n° 18/00485”
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,…
…oduct, its normal or reasonably foreseeable use or its instructions for use, or with the special precautions for use referred to in point d of paragraph 1 of Article 19 of Regulation (EC) No 1223/2009…
…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 Director General of the Agence n…
…r possession must bear a label of a size appropriate to their volume, affixed in such a way that it cannot be accidentally detached. This label bears, in indelible and legible black characters, the fo…
…authority of the exporting third country that:1° The standards of good manufacturing practice applicable to the establishment manufacturing the exported active substances are at least equivalent to t…
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…
…this interview is to enable the nurse to assess whether the student's situation corresponds to the cases of emergency mentioned in the third paragraph of I of article L. 5134-1. The medicinal product…
…used, suspended or withdrawn by the Director General of the Agency. Decisions to refuse, suspend or cancel registration are notified to the applicant. Reasons are given for the decision and the applic…
Decisions to register homeopathic veterinary medicinal products or to suspend or cancel these registrations are made public in an extract on the website of the Agence nationale de sécurité sanitaire d…
Medicinal products subject to clinical trials, on the one hand, and any reference medicinal products and placebos, on the other, are prepared in accordance with good manufacturing practice, defined in…
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