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This study was authorised by Italian Ministry of Health.
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All patients gave their informed consent for surgery, and the study was authorised by the local ethical committee.
(1) The patients gave informed consent prior being included into the study, (2) the study was authorised by the local ethical committee and was performed in accordance with the ethical standards of the 1964 Declaration of Helsinki as revised in 2000.
Informed consent was obtained from all participants and the study was authorised by the ethics committee of the Faculté des Sciences de la Santé at the Université d'Abomey-Calavi in Benin.
Additionally, the study was authorised by the Paul-Ehrlich-Institut (as an agency of the German Federal Ministry of Health) and by the German Federal Authorities for Radiation Protection (Bundesamt für Strahlenschutz) according to federal law.
The study was authorised by the local ethical committee and was performed in accordance with the Ethical standards of the 1964 Declaration of Helsinki as revised in 2000.
The study was authorised by the Local Institutional Animal Care Committee (Munkahelyi Állatjóléti Bizottság, MÁB) (no. 51/2013).
The study was authorised by the veterinary office of the Canton of Zurich (permit number 26/2014).
The study was authorised by the local ethical committee (No. 95/07).
The study was authorised by Herault and Gard Prefectures, Ministère de l'Ecologie et du Développement Durable, and Conseil National de Protection de la Nature, as well by the Montenegrian Institute for Natural Conservation.
The study was authorised by the French (Agence Nationale du Médicaments Vétérinaire, authorization # EC/05/043) and United Kingdom (UK) (Veterinary Medicines Directorate, Animal Test Certificate Vm12501/0038) regulatory authorities and internal Novartis reviews based on scientific, ethical and animal welfare guidelines.
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