Примери за използване на Authorisation holder на Английски и техните преводи на Български
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Medicine
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Colloquial
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Ecclesiastic
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Ecclesiastic
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Computer
Where the authorisation holder refuses its consent,
The authorisation holder can apply for the renewal of an authorisation to the Member State competent authority(MSCA)
they shall inform if necessary the authorisation holder and request him to change the labelling accordingly.
To this end, the authorisation holder must‘record and report all suspected adverse reactions in humans,
The single master file shall be addressed to the competent authority of the Member State in which the qualified person designated by the authorisation holder conducts the operations described in this file.
accurate information for each medicinal product is its marketing authorisation holder.
Manufacturing Authorisation holder responsible for batch release Roche Pharma AG,
where the authorisation holder is currently established in the United Kingdom.
The Marketing Authorisation Holder must implement nationally, prior to marketing, and as agreed with the competent authorities in the Member States.
The Marketing Authorisation Holder(MAH) shall provide an educational pack covering the therapeutic indications RA
To this end the authorisation holder shall record and report all suspected adverse reactions in humans,
75 thereof, on behalf of a marketing authorisation holder.
The authorisation holder shall submit to the Commission annual reports on the implementation
To this end, the authorisation holder shall record and report all adverse reactions,
the competent authorities or the Commission or undertaken in cooperation with the manufacturer of the veterinary medicinal product in question or marketing authorisation holder.
monitoring arrangements related to the management, the authorisation holder must submit an update of the exposure scenarios in the CSR.
semi-trailer is not registered in the name of the authorisation holder or if it is registered in another country.
was recorded in R4BP2, this means that the record of your authorisation in R4BP2 did not contain a valid LE UUID for the authorisation holder.
Commission, shall revoke the marketing authorisation if the marketing authorisation holder no longer fulfils the requirement on establishment in the Union,
If the composition of a new product falls within these established ranges an authorisation holder only needs to notify the product to the authorities 30 days before placing the new product on the market.