Article R123-208-3
…eclaration provided for in Article L. 123-29 is sent by registered letter with acknowledgement of receipt or delivered against receipt.If the application is incomplete, the regional chamber of commerc…
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Showing 3271–3280 of 34678 articles for “Art. CE 27-3-2020 n° 428234”
…eclaration provided for in Article L. 123-29 is sent by registered letter with acknowledgement of receipt or delivered against receipt.If the application is incomplete, the regional chamber of commerc…
…sentation of a statement of expenses and is limited, per month, to the amount of the maximum allowance likely to be paid to the mayor of a municipality of less than 500 inhabitants pursuant to the sca…
…dentiel et de résolution shall consult the competent authorities of the home country of the firm. Once the on-site inspection has been completed, the AMF shall promptly provide the competent authoriti…
…ee mentioned in Article R. 1432-78 in proportion to the number of staff on each college, in accordance with the first and fourth paragraphs of Article R. 1432-86. Staff representation on the Agency Co…
…ntative of the State in the department by this chapter are exercised in Paris by the Prefect of Police.
…ng information: 1° The holder's birth name and, where applicable, surname, first names, date and place of birth, nationality, home address; 2° The unique identification number (SIREN) of the company o…
…it has or becomes aware of which could lead to a change in the assessment of the risk-benefit balance of the medicinal product or product as defined in the first paragraph of Article L. 5121-9. It sh…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may require samples and mock-ups to be submitted when the medicinal product is marketed.
The marketing authorisation issued by the Agence nationale de sécurité du médicament et des produits de santé lapses if it transpires that: 1° That it is not followed by the marketing of the medicinal…
…lementation of measures to ensure the safe use of the medicinal product or product; 2° The performance of post-authorisation safety studies; 3° Compliance with specific obligations regarding the recor…
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