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Showing 1001–1010 of 54531 articles for “Art. Loi 2019-744 of 19 July 2019”
…tres inform the Agence nationale de sécurité du médicament et des produits de santé on the same day of the reports of adverse reactions likely to be due to a blood-derived medicinal product that they…
…respondent mentioned in article R. 5121-181 who receives the report provided for in article R. 5121-196 immediately forwards it to the regional pharmacovigilance centre. If he is otherwise aware of an…
Organisations or companies exploiting blood-derived medicinal products which have knowledge of adverse reactions likely to be due to these medicinal products inform the Director General of the Agence…
When a person authorised to prescribe, dispense or administer medicinal products becomes aware of an adverse reaction which may be due to a blood-derived medicinal product, he/she shall report it imme…
All pharmaceutical acts are carried out under the effective control of a pharmacist who meets the conditions for practising pharmacy in France.
…articles R. 5122-5 to R. 5122-7. The approval confers no guarantee as to the properties and effects of the product. It is granted for a period which may not exceed five years.
The direct or indirect holding of shares representing all or part of the share capital of a société d'exercice libéral de pharmaciens d'officine by a natural or legal person practising a liberal healt…
I.-The administrative authority referred to in the first paragraph of article L. 6323-17-6 is the regional prefect.II-The regional joint cross-industry committee provided for in article L. 6323-17-6 i…
In the event of suspension of the employment contract with total or partial retention of the employee's gross monthly remuneration, the number of paid hours taken into account for the calculation of t…
Without prejudice to the provisions of I of article L. 822-1 of the French Commercial Code applicable to public limited companies, private-sector training providers must appoint at least one statutory…
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