Article R5133-5
Where it appears that a reagent presents risks to public health, including as a result of non-compliance with the rules laid down in this chapter, the Director General of the Agence nationale de sécur…
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Showing 4971–4980 of 6073 articles for “Art. 28 March 2012”
Where it appears that a reagent presents risks to public health, including as a result of non-compliance with the rules laid down in this chapter, the Director General of the Agence nationale de sécur…
In the event of a serious adverse reaction likely to be due to a tattooing product, the persons responsible for placing a tattooing product on the market, the health professionals who have observed it…
The decision to administer emergency contraception is preceded by an interview with the student, whether she is a minor or an adult. The purpose of this interview is to enable the nurse to assess whet…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail may automatically vary a marketing authorisation for a veterinary medicinal produ…
Advertising of veterinary medicinal products to the natural or legal persons mentioned in article R. 5141-83 must include at least the following information: 1° The name of the medicinal product ; 2°…
Advertising for ... is subject to prior authorisation from the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail: 1° Antibiotics ; 2° V…
As part of the EC declaration of conformity procedure, the manufacturer shall draw up technical documentation making it possible to assess the conformity of the medical device with the essential requi…
For Class IIa medical devices or Class I medical devices, the provisions of Article R. 5211-43 apply subject to the following modifications: 1° For class II a medical devices, the authorised body veri…
Automated external defibrillators, which for the purposes of this section are fully automatic external defibrillators and semi-automatic external defibrillators, are a medical device authorised to be…
I.-In the organisations referred to in article R. 6325-1, the holding, control, management and dispensing of medicinal products are carried out by a pharmacist registered on the roll of the competent…
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