Article R5121-107-15
If, after a traditional herbal medicinal product has been registered, the proprietor considers, on the basis of new data available to him, that, given its characteristics, the medicinal product is now…
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Showing 2861–2870 of 31982 articles for “Art. 10 May 2017”
If, after a traditional herbal medicinal product has been registered, the proprietor considers, on the basis of new data available to him, that, given its characteristics, the medicinal product is now…
…ist by the Commission, the information and documents mentioned in 5°, 6° and 16° of Article R. 5121-107-4.
I.-The Director General of the Agence nationale de sécurité du médicament et des produits de santé publishes, on the Agency's website, a reference database of medicinal products which are the subject…
The following changes to the authorisation to open a pharmaceutical establishment must be declared, pursuant to the second paragraph of Article L. 5124-3: 1° Change in the corporate name of the compan…
The Board comprises : 1° Four representatives of the State, including the Regional Prefect and three representatives appointed by him from among those mentioned in 2° of Article R. 6123-3-3, including…
Requests for professional transition leave which cannot all be satisfied by the employer are considered in the following descending order of priority: 1° Requests which have already been submitted and…
I.-The beneficiary of the professional transition leave provides the employer with supporting documents, drawn up by the training organisation, proving his/her attendance at the training course at the…
I.-The approved cross-industry skills operators concerned are invited, by means of a call for applications, to send the ministers responsible for vocational training and the overseas departments and t…
The licence application must include : 1° The company's unique identification number, together with its articles of association if it is a legal entity; 2° A curriculum vitae indicating, in particular…
Tattoo products are subject to vigilance designed to monitor undesirable effects occurring under normal conditions of use of the product or resulting from misuse. This vigilance is applied to all thes…
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