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Showing 3951–3960 of 32219 articles for “Art. Décret 87-713 du 26-8-1987”
A proprietary medicinal product covered by the regulations on poisonous substances may not be unpackaged by the dispensing pharmacist with a view to its incorporation into a magistral preparation.This…
…ean Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use.
…neral of the Agency in the following cases: 1° When the use of the micro-organisms and toxins or products containing them mentioned in this authorisation no longer complies with the provisions of this…
…irection of existing facilities for obtaining such medication: pharmacy, planning centre or family education centre. The nurse may administer emergency contraception to the student concerned in order…
The purpose of veterinary pharmacovigilance is to monitor the effects of veterinary medicinal products, mainly their adverse effects on animals and humans, and the scientific evaluation of information…
Each committee comprises : 1° Three representatives of the State and one representative of the Regional Health Agency: a) The Regional Prefect or his representative, Chairman ; b) The Regional Directo…
If a medical device is intended to be used in conjunction with another medical device, the classification rules apply separately to each device. Computer software controlling a device or influencing i…
…anied by a daily penalty payment. This penalty payment is notified in accordance with the same procedural rules as the main sanction. The amount of the daily penalty is calculated from the date of not…
Without prejudice to the provisions of Article R. 5221-9, in vitro diagnostic medical devices which comply with the standards relating to them and transposing the harmonised European standards, the re…
The authorisation is issued for a period of five years. At the request of the holder, submitted no later than two months before the normal expiry date, the initial authorisation is renewed for a perio…
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