Article R5125-12
…rofessions in accordance with the laws and regulations in force. The applicant may not practise the dual profession until he or she has received a certificate from the Director General of the Regional…
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Showing 2981–2990 of 30105 articles for “Art. Décret 2015-1763 du 24-12-2015”
…rofessions in accordance with the laws and regulations in force. The applicant may not practise the dual profession until he or she has received a certificate from the Director General of the Regional…
An in-house pharmacy may be authorised to have premises located on several separate sites belonging to one or more of the establishments, services or organisations mentioned in Article R. 5126-1, prov…
A quantity of medicinal products corresponding to a treatment period of more than four weeks or one month of thirty days, depending on the packaging, may not be dispensed on a single occasion. However…
One of the samples is left with the owner or holder of the product. If the interested party refuses to keep the said sample on deposit, this refusal will be mentioned in the report or the minutes. Und…
Advertising to the public for a product or object defined in article R. 5134-11 :1° Is designed in such a way that the advertising nature of the message is obvious ;2° Contains at least :a) The name o…
…eads as follows: "When a person who keeps animals belonging to one of the species whose flesh or products are intended for human consumption plans to carry out medicinal product trials other than thos…
…or records mentioned in articles R. 5141-118 to R. 5141-120 are kept for five years and must be produced whenever required by the competent authorities. The recording systems comply with the characte…
A veterinary surgeon who prescribes medicinal products containing substances having an oestrogenic, androgenic or gestagenic action for farm animals shall record the following information in chronolog…
…f Article L. 241-3 of the Rural and Maritime Fishing Code may use in France veterinary medicinal products other than immunological medicinal products which have been granted a marketing authorisation…
Any medical device placed on the market or put into service in France must bear the CE mark certifying that it meets the conditions set out in article R. 5211-17. However, CE marking is not required f…
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