Examples of using Master file in English and their translations into Swedish
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
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Programming
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Political
include a reference to the site where the Pharmacovigilance System Master File for the medicinal product concerned is maintained and accessible for inspection.
as applicable, may at any time request the marketing authorisation holder to submit a copy of the pharmacovigilance system master file.
A Vaccine Antigen Master File means a stand-alone part of the marketing authorisation application dossier for a vaccine,
To this end the concept of a plasma master file(PMF) should be introduced, in particular in order to allow the pooling of national expertise and through the coordination by the EMEA of a single evaluation.
This Regulation also applies for the examination of applications of variations to the terms of a plasma master file and of a vaccine antigen master file,
The NanoHorizons Device Master File provides technical,
Many Ehrenberg-Bass master file templates- such as those used for business proposals- reside in Dropbox, so it's often
Many Ehrenberg-Bass master file templates- such as those used for business proposals- reside in Dropbox, so it's often the starting point for professors, honor students,
Please note that depending on which country the activities are performed in, foreign companies may have an obligation to prepare and submit the Master File and Local File as soon as 2017.
content of the pharmacovigilance system master file and its summary.
is that the marketing authorisation holder does not comply with the pharmacovigilance system as described in the pharmacovigilance system master file and with Title IX,
How can I convert. master files to another format?
A list of the locations in the Community where pharmacovigilance system master files are sited
The marketing authorisation holder shall have in place one or more pharmacovigilance system master files describing in detail the pharmacovigilance system with respect to its authorised veterinary medicinal products.
In clinical medicine studies, Trial Master Files(TMF), one for the clinical investigator and one for the sponsor,
delegation of responsibilities between competent authorities shall ensure that there is no duplication of inspections of pharmacovigilance system master files.
render out precisely optimized master files.
The competent authorities of the Member States in which the pharmacovigilance system master files are located shall carry out inspections of the pharmacovigilance systems master files.
The pharmacovigilance inspections shall be coordinated by the Agency together with the competent authorities and shall ensure that all pharmacovigilance system master files in the Union, as identified in the product database,
Updates to a-blogsite may change the code in master files but you can always compare your custom templates to master files