Voorbeelden van het gebruik van Marketing authorization in het Engels en hun vertalingen in het Nederlands
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Programming
Applications for registration or for marketing authorization for medicinal products covered by this Directive lodged after the date set in paragraph 1 shall comply with the provisions of this Directive.
Whereas marketing authorization shall be refused where a medicinal produci lacks therapeutic effect
This fee shall be deducted from that charged for a marketing authorization for a medicinal product containing the substance where such authorization is applied for by the undertaking originating the establishment of the MRL.
In addition, the Community rules lay down that examination of an application for marketing authorization under the conciliation procedure should nor exceed 210 days,
The marketing authorization holder shall establish within his undertaking a scientific service in charge of information about the medicinal products which he places on the market.
Sun holds a marketing authorization for generic zoledronate 5 mg/100 ml for the treatment of both osteoporosis
Marketing authorization should be refused where a medicinal product lacks therapeutic effect
If a marketing authorization were to be issued by the MCA,
changes In technical or other arrangements should be in accordance with the marketing authorization for the product concerned.
Not inappropriately restricting the ability of marketing authorization holders to provide in an understandable way objective
Before any Member State takes a decision on an application for marketing authorization or a decision to withdraw
importer, marketing authorization holder, or wholesale distributor concerned the opportunity to submit their comments.
The Member States shall either grant or withdraw marketing authorization, or vary the terms of a marketing authorization as necessary to comply with the decision within 30 days of its notification.
When applying for marketing authorization the producer must provide information concerning the characteristics of the product,
This is the fee for review of the available new information about the medicinal product at the time of the obligatory five-yearly renewal of a Community marketing authorization for that product granted for each strength and/or pharmaceutical form.
When applying for marketing authorization the producer must provide information concerning characteristics of the products,
refusal or withdrawal of marketing authorization.
may submit authorization holder of the marketing authorization.
When seeking marketing authorization for a new pharmaceutical producers have to provide detailed results of tests performed,
competent authorities and the holder of marketing authorization of the original product should be informed immediati}·.