Article L5142-6-1
Persons providing information by canvassing or canvassing for veterinary medicinal products are required to satisfy qualification conditions defined by decree, which guarantee that they have sufficien…
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Showing 9801–9810 of 61436 articles for “Art. L 227-20-1”
Persons providing information by canvassing or canvassing for veterinary medicinal products are required to satisfy qualification conditions defined by decree, which guarantee that they have sufficien…
Parallel trade in a veterinary medicinal product under the conditions provided for in Article 102 of Regulation (EU) 2019/6 of 11 December 2018 is subject to authorisation by the Director General of t…
The preparation of veterinary medicinal products not falling within the scope of Regulation (EU) 2019/6 of 11 December 2018, excluding extemporaneous preparations, is carried out by a qualified person…
Tattoo products must be manufactured in accordance with good manufacturing practice, the principles of which are defined by order of the ministers responsible for consumer affairs and health, issued o…
The dispensing of certain medicinal products by pharmacists or veterinary surgeons, where their pharmaceutical form so permits, may be by the unit, provided that the integrity of the immediate packagi…
The local or regional representative referred to in paragraph 3 of Article 77 of Regulation (EU) 2019/6 of 11 December 2018 shall carry out his duties in professional premises located on national terr…
Transplantation of faecal microbiota is carried out in the interests of the recipient and is subject to the principles of donor consent and anonymity of donation. The rules of anonymity of donation do…
The person responsible for placing a tattoo product on the market is required, in the event of serious doubt as to the harmlessness of one or more substances, to provide the Director General of the Ag…
Tattoo products placed on the market must not harm human health when applied under normal or reasonably foreseeable conditions of use, taking into account, in particular, the presentation of the produ…
I.-The criteria for classifying a situation as a risk in the management of a patient's state of health due to the unavailability of a medical device shall be laid down by regulation.The manufacturers…
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