Examples of using Master file in English and their translations into Slovak
{-}
-
Colloquial
-
Official
-
Medicine
-
Financial
-
Ecclesiastic
-
Official/political
-
Computer
-
Programming
of paragraph 1g◄ 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, the competent authority
the Reporting New Zealand Financial Institution must also review the current customer master file and, to the extent not contained in the current customer master file,
a High Value Account, the Reporting Financial Institution must also review the current customer master file and, to the extent not contained in the current customer master file,
the Reporting New Zealand Financial Institution must also review the current customer master file and, to the extent not contained in the current customer master file, the following documents
The two-story structure at the center of the complex… houses a hard drive with his master files.
This generates a new. master file.
Archiving of the clinical trial master file.
Correcting errors in the master file table's(MFT) BITMAP attribute.
Plasma Master File Vaccine Antigen Master File.
Any alteration to the content of the clinical trial master file shall be traceable.
The Plasma Master File shall be updated
Any transfer of ownership of the content of the clinical trial master file shall be documented.
The authorisation holder shall also submit to the competent authority any substantive changes to his single master file.
Chkdsk ensures only that the Master File Table(MFT) has entries for these files and that the entries are valid entries.
Working directly on the Master File Table of the NTFS partitions,
Orion as a marketing authorization holder maintains pharmacovigilance system which needs to be documented in Pharmacovigilance System Master File(PSMF).
To be supplied in a separate document directly to the competent authorities by the manufacturer of the active substance as an Active Substance Master File.
requirements for the contents of the master file and investigational medicinal product traceability.
Any marketing authorisation dossier containing a human plasma-derived constituent shall refer to the Plasma Master File corresponding to the plasma used as a starting/raw material.
The content of the clinical trial master file shall be archived in a way that ensures that it is readily available, upon request, to the competent authorities.