Примери за използване на Application dossier на Английски и техните преводи на Български
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Part IV of the application dossier; c an Assessment of the Periodic Safety Update Reports(PSURs) in relation to target animal safety
The evaluating competent authority is responsible for carrying out the validation of the application dossiers and subsequently for the evaluation of the dossiers submitted by the applicants.
The reference MSCA is responsible for carrying out the validation of the application dossiers and for the evaluation of the dossier submitted by the applicant
The reference competent authority is responsible for carrying out the validation of the application dossiers and for the evaluation of the dossier submitted by the applicant in case of mutual recognition renewal.
An application dossier as referred to in Article 24(7) shall include.
In such case, the application dossier referred to in Article 23(2)
the sponsor shall submit an application dossier to the Member States concerned through the EU portal.
importers must supply an application dossier to the Agency in which the data and the determinations have been documented.
text is in the original application dossier;
Where a clinical trial has more than one sponsor, detailed information of the responsibilities of each of the sponsors shall be submitted in the application dossier.
A sponsor shall not submit an application dossier in accordance with this Article where a procedure set out in Chapter III is pending as regards that clinical trial.
The application dossier for the authorisation of a substantial modification shall contain all required documentation
The application dossier and any data added to it up to Day 60 of the referral procedure in CMD(v)
an indication as to where the relevant information or text is located in the original application dossier;
which was not included in Part IV of the application dossier.
The application dossier for the authorisation of a clinical trial shall contain all required documentation
The cover letter shall indicate the location in the application dossier of the information necessary for assessing whether an adverse reaction is a suspected unexpected serious adverse reaction,
Guidelines addressed to the Member States for the presentation of an application dossier are contained in Council Directive 87/153/EEC of 16 February 1987 fixing guidelines for the assessment of additives in animal nutrition(11).
Module 5(Clinical Study Reports) of the marketing authorisation application dossier.
which was not included in Part IV of the application dossier.