Examples of using Non-interventional in English and their translations into German
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Non-interventional post-authorisation safety study PASS.
The person responsible for the NIS(Verantwortlicher) is the person in whose name the non-interventional study will be conducted.
Every non-interventional study is assigned a unique notification number that cannot be changed.
Codification of guiding principles and oversight for the conduct of non-interventional post-authorisation safety studies;
Information on non-interventional studies performed by Bayer is available at www.clinicaltrials.gov.
A Japanese pharmaceutical company in the area of pharmaceutical compliance and clinical trials as well as non-interventional studies.
Non-interventional studies and studies not controlled by the Medicines Act do not have a EudraCT number.
The use of the Internet enables a more efficient approach to conducting non-interventional studies(NIS) as well as studies and clinical evaluations of medical products.
Non-interventional trial": a study where the medicinal product(s) is(are) prescribed in the usual manner in accordance with the terms of the marketing authorisation.
The NIS notification number(NIS-Meldenummer)serves the purpose of unequivocally identifying a non-interventional study in the electronic NIS notification system of the BASG currently only available in German.
Clinical trials, non-interventional studies, non-clinical data, other periodic reports, lack of efficacy in controlled clinical trials, overview of signals.
In particular, it asks the Commission to check on the various translations of the term"non-interventional clinical trials", as the present translations could give rise to misunderstandings.
A non-interventional study to evaluate the occurrence of neurological and ophthalmic adverse events(to be coded using the relevant Veddra terminology) in dogs treated with Trifexis.
The internet is the ideal solution for the efficient implementation of NIS(non-interventional studies) as well as for general clinical surveys and reviews of medical products.
Non-interventional studies(NIS) have proven to be useful tools for examining the safety, effectiveness and tolerability of a marketed medical product as it is used in day-to-day practice.
A further useful classification of study types in clinical andepidemiological research is interventional and non-interventional(NIS) or observation studies.
The activities encompass clinical trials and non-interventional studies in hospitals and medical practices in Germany and other European countries, especially Austria and Switzerland.
There are considerable doubts as to whether patientsare capable of correctly evaluating information on non-interventional scientific studies and drawing the necessary conclusions.
The EESC urges that information on non-interventional scientific studies not be considered as information which can be disseminated to the public, and that the relevant sections of the proposal be deleted.
The following sections list less common data available for homeopathic products:Clinical trials, non-interventional studies, non-clinical data, other periodic reports, lack of efficacy in controlled clinical trials, overview of signals.
The beginning of a non-interventional study within the meaning of Art 8 of the Ordinance of the Federal Minister of Health on the Notification Requirement for Non-Interventional Studies is defined as the day the first patient is enrolled into the study.
The legal proposal foresees that the EMEA shall be charged with supervision of specific pieces of information on centrally authorised products:Medicinal product-related information about non-interventional scientific studies or accompanying measures to prevention and medical treatment, or information which presents the medicinal product in the context of the condition to be prevented or treated shall be notified to the EMEA prior to publication in health-related publications or in an Internet site.
Non-interventional studies on drugs in current therapeutic practice are based on a large number of patients and provide indispensable scientific insights into the acceptance and practicability of a medicine, on possible interactions with other drugs, previously unknown, very rarely occurring side effects and possible new findings on efficacy.
This should cover medicinal product-related information about non-interventional studies, or accompanying measures to prevention and medical treatment, or information which presents the medicinal product in the context of the condition to be prevented or treated.
This concerns information about non-interventional scientific studies, or accompanying measures to prevention and medical treatment, or information which presents the medicinal product in the context of the condition to be prevented or treated.
Given that the EESC isnot in favour of disseminating information on the results of non-interventional studies or of using"health-related publications" as a means of dissemination, a rethink is needed of the idea of requiring information to be checked prior to its dissemination as provided for under Article 100g1.
This Chapter shall apply to non-interventional post-authorisation safety studies which are initiated, managed or financed by the marketing authorisation holder, voluntarily or following a requirement in accordance with Articles 21a or 22a, and which involve the collection of data from patients or health-care professionals.
PROGNOSIS was a multi-center, prospective, double-blind, non-interventional trial evaluating the short-term prediction of preeclampsia, eclampsia and HELLP(hemolysis, elevated liver enzymes, low platelet count) syndrome in pregnant women with suspected preeclampsia.
Medicinal product-related information about non-interventional scientific studies, or accompanying measures to prevention and medical treatment, or information which presents the medicinal product in the context of the condition to be prevented or treated.
Harmonised guiding principles and a procedure for the supervision of non-interventional post-authorisation safety studies(i.e. safety studies of authorised products that are not clinical trials), in particular to ensure that they are non promotional, and the follow-up of any safety data generated in such studies.