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Showing 6421–6430 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
…522-1 of the Environment Code" are replaced by the words: "of locally applicable regulations on the marketing and use of biocidal products".
…es produits de santé may require samples and mock-ups to be submitted when the medicinal product is marketed.
As part of an operation to monitor the routing or transport of objects, goods or products derived from the commission of a customs offence or used to commit a customs offence, where the prison sentenc…
Pharmacovigilance of blood-derived medicinal products involves monitoring, known as traceability, from the time they are manufactured until they are administered to patients. The purpose of this monit…
When a person authorised to prescribe, dispense or administer medicinal products becomes aware of an adverse reaction which may be due to a blood-derived medicinal product, he/she shall report it imme…
…or General of the Agency for the purposes of research and control and the manufacture of authorised derivatives.
The commission draws up its own rules of procedure, which specify in particular the rules for preventing conflicts of interest. These rules are applicable once they have been approved by the France Co…
…rvices and amending Regulation (EU) No 1024/2012 on administrative cooperation through the Internal Market Information System ("IMI Regulation").The penalty or fine is recovered in accordance with the…
…economic interest groups, the creation of subsidiaries and the acquisition of financial holdings;9° Rules relating to contracts and markets;10° The annual report referred to in the last paragraph of a…
The booklet of rules summarises the rules enacted by the plan to implement the development guidelines and principles and contribute to achieving the objectives provided for in the second to fourth par…
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