Examples of using Authorization holder in English and their translations into Polish
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Financial
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Official/political
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Programming
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Computer
Marketing Authorization Holder and Manufacturer.
Name or corporate name and permanent address of the marketing authorization holder.
Within 15 days of the receipt of the opinion, the marketing authorization holder may notify the Agency in writing of his intention to appeal.
registered place of business of the authorization holder.
In order for the safety features to be effective, the manufacturing authorization holder should only be permitted to remove,
People also translate
2 shall be borne by the authorization holder or his representative.
Allowing marketing authorization holders to provide in an understandable way objective
where appropriate, of the authorization holder.
Not inappropriately restricting the ability of marketing authorization holders to provide in an understandable way objective and non-promotional information about the benefits
registered place of business of the marketing authorization holder and of the manufacturer, if different;
Member States may require the marketing authorization holder for immunological veterinary medicinal products to submit to the competent authorities copies of all the control reports signed by the qualified person in accordance with Article 55.
referred to in paragraph 1 in order to allow the marketing authorization holder to prepare explanations.
A copy of the renewal application, together with the dossier, shall be officially forwarded by the authorization holder via the Member State acting as rapporteur to the other Member States, which shall acknowledge
where applicable, of the marketing authorization holder.
The marketing authorization holder for immunological veterinary medicinal products shall ensure that an adequate number of representative samples of each batch of veterinary medical products is held in stock at least up to the expiry date,
A decision as referred to in paragraph 1 shall be addressed to the Member States concerned by the matter and communicated to the marketing authorization holder.
Where, for reasons beyond the control of the authorization holder, no decision may be taken on the renewal application before the expiry date of the authorization,
registered place of business of the marketing authorization holder and of the manufacturer, if different;
alter the general legal liability of the manufacturer or as appropriate the marketing authorization holder.
importer, marketing authorization holder, or to the wholesale distributor who has undergone the inspection.
the other Member States and the marketing authorization holder.
travel authorization no longer apply, or if the travel authorization holder is found to have violated any of the ETIAS rules.
concerned by the application, the Agency, and the marketing authorization holder.
carried out in cooperation with the manufacturer or marketing authorization holder for the medicinal product concerned;
which is referred to the Committee for consideration and shall inform the marketing authorization holder.
84 or on whether the marketing authorization holder complies with the requirements laid down in Title IX.