Article D4364-12
Orthoprosthetists, chiropodists, ocularists, epithesists and orthopaedic orthotists are bound by professional secrecy under the conditions and subject to the penalties set out in articles 226-13 and 2…
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Showing 2081–2090 of 48499 articles for “Art. Cass. soc. 25 October 2006 · Cass. soc. 8 October 2003 · Cass. soc. 12 February 1985 · Cass. soc. 16 October 1984 · Cass. soc. 12 October 2004 · Cass. soc. 9 June 1983 · Cass. soc. 23 February 1977 · Cass. soc. 28 May 1997 · Cass. soc. 19 January 2011”
Orthoprosthetists, chiropodists, ocularists, epithesists and orthopaedic orthotists are bound by professional secrecy under the conditions and subject to the penalties set out in articles 226-13 and 2…
The people who direct and supervise the performance of chemical, pharmaceutical, biological, pharmacological or toxicological tests are known as experimenters.
…ation is granted for a period of five years. It specifies the differences mentioned in articles R. 5121-117 to R. 5121-119 with the speciality that has obtained marketing authorisation in France. It i…
…sation period. Renewal of the authorisation is granted under the conditions set out in Articles R. 5121-116 and R. 5121-123. If the Director General of the Agence nationale de sécurité du médicament e…
…by weight, volume or number of dosage units, as well as the name within the meaning of Article R. 5121-1 and the contents of the packaging of the proprietary medicinal product as it will be marketed…
…thorisation to open the establishment authorised within the meaning of Article 40 of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relatin…
The holder of a parallel import authorisation notifies the holder of the marketing authorisation for the proprietary medicinal product in the Member State of origin of the marketing in France of the p…
…duct benefiting from the parallel import authorisation complies with the provisions of Articles R. 5121-118, R. 5121-119 and R. 5121-128.
For each parallel import operation, the authorisation holder notifies the Director General of the Agence nationale de sécurité du médicament et des produits de santé of the batch numbers of the author…
…thorisation in France;-the classification of the product in the categories mentioned in article R. 5121-36.
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