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Showing 3741–3750 of 11432 articles for “Art. CE 17-10-1990 n° 56991”
…ion has been granted, which could lead to a change in the registration dossier. This information concerns in particular the assessment of the quality, safety and homeopathic use of the medicinal produ…
After registration, manufacturing methods and control techniques take account of scientific and technical progress. Any resulting changes must first be registered under the conditions set out in artic…
A medicinal product or a series of medicinal products mentioned in Article L. 5121-13 may only be registered if the applicant is established in a Member State of the European Community or a party to t…
…is suspended or withdrawn, the holder informs the stockholders without delay. They must take all necessary steps to stop the distribution of the medicinal product. If these steps are not taken within…
Registration of homeopathic medicinal products and traditional herbal medicinal products, as well as suspension and withdrawal of registration, are made available to the public by the Director General…
When a medicinal product is subject to the restricted prescription conditions laid down in section 8 of chapter I of this title, it may only be advertised to prescribers authorised to draw up the pres…
Authorisations to set up, transfer or group pharmacies are subject to compliance with the conditions set out in articles R. 5125-8 and R. 5125-9 and in 2° of article L. 5125-3-2.
…r in 2° and 3° of Article L. 5126-1. Clinical pharmacy activities are as follows: 1° Clinical pharmaceutical appraisal of prescriptions involving medicinal products, products or objects mentioned in a…
The Executive Committee meets at least once a year, convened by its Chairman who sets the agenda.
…the managing body of any termination, suspension or modification of the young people's work experience contract that gives rise to entitlement to the aid, resulting in a change in the amount of the ai…
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