Article L444-4
Commissaires de justice, administrateurs judiciaires, mandataires judiciaires, the persons mentioned in the second paragraph of
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Showing 4791–4800 of 58536 articles for “Art. II · Cass. 3e civ. 15 September 2010 · Cass. 3e civ. 4 November 1998”
Commissaires de justice, administrateurs judiciaires, mandataires judiciaires, the persons mentioned in the second paragraph of
The other provisions of Title II of Book VII relating to the commercial courts are applicable to the commercial chamber, with the exception of articles L. 721-1, L. 721-2, L. 722-3, and L. 722-11 to L…
…their joint authority, he is responsible for implementing the missions mentioned in Article L. 612-47.II. - The authorities shall make available to the coordinator and to persons working in the conte…
Referral to the judicial court pursuant to II of article L. 2331-1 must be made within three months of the notification provided for in article R. 2331-1, failing which the case will be inadmissible.…
…pproved laboratory shall immediately inform the public establishment referred to in Article L. 3512-15 of any situation that may no longer enable it to comply with one or more conditions of approval.…
Manufacturers of medicinal products referred to in article R. 5124-2 shall check that the active substances used come from manufacturers, importers or distributors either authorised by the Agence nati…
Manufacturers of medicinal products must be able to document the measures they have taken to ensure that their supplier of excipients complies with good practice under the conditions set out in articl…
I.-For the medicinal products of major therapeutic interest referred to in article L. 5111-4, marketing authorisation holders and pharmaceutical companies exploiting medicinal products shall, under th…
…rom two companies engaged in the distribution of medicinal products as referred to in article R. 5124-2. This 72-hour period may be reduced at the pharmacist's initiative, depending on compatibility w…
…horised under Article 13.1 of Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001. In the case of reference medicinal products benefiting from a marketing authorisation…
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