Примери за използване на Particulars and documents на Английски и техните преводи на Български
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Ecclesiastic
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the importer from a third country is able to manufacture the medicinal product concerned and/or carry out the necessary control tests in accordance with the particulars and documents supplied pursuant to Article 6.
(a) the particulars and documents.
The following particulars and documents shall accompany an application in accordance with Annex I.
Annex I shall apply by analogy to the particulars and documents specified in point(a).
the applicant shall send the following particulars and documents directly to the Authority.
The CHMP considers that at present, the particulars and documents provided for in Article 8(3)
Submit immediately to the FDA any new information which might entail the amendment of the particulars and documents referred to in art.
Authorisation shall likewise be refused if the particulars and documents submitted in support of the application do not comply with Articles 8 and 10(1).
which shall conform with the particulars and documents provided pursuant to Articles 12 to 13d
including the particulars and documents referred to in paragraph 3,
The CHMP considers that in the absence of GMP compliance of the manufacturing site Pharmaceutics International Inc., the particulars and documents provided for in Article 8(3)
The CHMP considers that in the absence of GMP compliance of the manufacturing site Pharmaceutics International Inc., the particulars and documents provided for in Article 8(3)
(a) shall verify that the particulars and documents submitted in accordance with Article 6 comply with the requirements of Directive 2001/83/EC,
(a) shall verify that the particulars and documents submitted in accordance with Article 28 comply with the requirements of Directives 81/851/EEC
In relation to the submission of certain documents and particulars there is a statutory requirement that the person making the submission must sign a statutory declaration that he or she believes that the required particulars and documents have been properly submitted.
These particulars and documents shall take account of the unique, Community nature of the authorisation requested
The particulars and documents accompanying the application for marketing authorization pursuant to Article 8(3)(h)
These particulars and documents shall take account of the unique,►M8 Union◄ nature of the authorisation requested
The particulars and documents accompanying the application for marketing authorization pursuant to Article 12(3)(i)
(26) Certain particulars and documents that are normally to be submitted with an application for a marketing authorisation shoulneed not be required if a veterinary medicinal product is a generic medicinal product of a veterinary medicinal product that is authorised or has been authorised in the Union.