Examples of using Performance study in English and their translations into Croatian
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Colloquial
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Ecclesiastic
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Computer
information about the availability of the performance study results in accordance with paragraph 6 of this Article.
Where the conclusion of the coordinating Member State concerning the area of coordinated assessment is that the performance study is not acceptable,
other than devices for performance study, shall be subject to a conformity assessment as specified in Chapters I,
(e) the performance study is essential with respect to incapacitated subjects
other than devices for performance study, may, instead of the conformity assessment procedure applicable pursuant to paragraph 3,
If a study is conducted in more than one Member State, the sponsor shall notify all Member States in which that performance study was conducted of the end of the performance study in all Member States.
of the comments or of the requested additional information, whether the performance study is considered as falling within the scope of this Regulation
within the performance evaluation, and any associated performance study, and appropriately guide external clinical experts in the assessment of the performance evaluation presented by the manufacturer;
which shall generate a Union-wide unique single identification number for the performance study which shall be used for all relevant communication in relation to that performance study.
informed consent to continue the participation in the performance study shall be obtained from the subject as soon as he or she is capable of giving informed consent.
informed consent before the onset of their incapacity, a performance study may be conducted only where,
where appropriate, any other person entitled by national law to provide the relevant patient care under performance study conditions;
The end of a performance study shall be deemed to coincide with the last visit of the last subject unless another point in time for such end is set out in the performance study plan.
A‘ clinical performance study report', signed by a medical practitioner
without having to provide any justification, withdraw from the performance study at any time by revoking his or her informed consent.
The summary and the performance study report referred to in paragraph 5 of this Article shall become publicly accessible through the electronic system referred to in Article 69, at the latest when the
If the device is not registered in accordance with Article 26 within one year of the summary and the performance study report having been entered into the electronic system pursuant to paragraph 5 of this Article, they shall become publicly accessible at that point in time.
informed consent in accordance with Article 59 shall be sought to continue the participation of the subject in the performance study, and information on the performance study shall be given, in accordance with the following requirements:(a).
(e) the performance study relates directly to the subject's medical condition because of which it is not possible within the therapeutic window to obtain prior informed consent from the subject or from his or her legally designated representative and to supply prior information, and the performance study is of such a nature that it may be conducted exclusively in emergency situations;
Where the Member State concerned finds that the performance study applied for does not fall within the scope of this Regulation or that the application is not complete,