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Showing 6101–6110 of 52212 articles for “Art. 1844-1”
The medical electroradiology manipulator is authorised to carry out, under the responsibility of the doctor referred to in article R. 4351-1, in application either of an individual medical prescriptio…
I.- When renewing an orthoptic prescription, the orthoptist may, after carrying out a refraction examination and unless the doctor expressly states otherwise on the prescription, adapt the optical cor…
The organisational protocol describes the medical situations concerned and the orthoptic procedures required.
When the protocol is used for the follow-up by the orthoptist of a patient whose visual pathology has already been diagnosed, without an ophthalmological examination being carried out on the same day,…
For its application in New Caledonia and French Polynesia, article R. 4234-1 in the version resulting from decree no. 2022-381 of 16 March 2022 reads as follows: Complaints and requests from the perso…
All medicinal products are fitted with the tamper-evident device referred to in Article R. 5121-138-2. However, this device is not compulsory for medicinal products on the list set out in Annex I to C…
I.-The outer packaging or, where there is no outer packaging, the immediate packaging of medicinal products bears safety features consisting of a unique identifier and a tamper-evident device, under t…
The safety features may only be replaced by equivalent safety features in order to verify the authenticity, identify and provide proof of unlawful handling of the medicinal product. This replacement i…
When a medicinal product is the subject of a reassessment of the risk-benefit balance, the Director General of the Agence nationale de sécurité du médicament et des produits de santé shall inform the…
In pharmaceutical establishments created within public establishments and non-profit organisations in application of article L. 5124-9-1, the legal representative of the legal entity concerned appoint…
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