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Before going into bioequivalence studies it is essential for the pharmaceutical industry to study the guidelines of bioequivalence for the respective country where the industry wants to market its products and thus enter into generic market.
In the current study, the guidelines of the 11th World Congress of Gastroenterology were followed in the evaluation of HE [ 16]; clinical assessment and simple bedside psychometric tests were chosen as they are easily applied in everyday practice.
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They were asked to study the national guidelines of the discipline.
This study met the guidelines of Capital Medical University, which abided by the Helsinki Declaration on ethical principles for medical research involving human subjects.
The study followed the guidelines of the Declaration of Helsinki.
The study followed the guidelines of the Declaration of Helsinki and was approved by the Regional Ethical Review Board in Stockholm (2009/2047-32), Sweden.
Both qualitative and quantitative interpretation of the CPT readings in this study followed the guidelines of DIN: 4094 Part 2 [10].
The study followed the guidelines of the European Communities Council (86/609/ECC) and was approved by the Ethics Committee of The Faculty of Medicine, University of Szeged, Hungary (I-74-12/2012).
The study followed the guidelines of the European Communities Council (86/609/ECC) and approved by the Ethics Committee of The Faculty of Medicine, University of Szeged, Hungary.
The study followed the guidelines of the European Communities Council (86/609/ECC) and approved by the Ethics Committee of The Faculty of Medicine, University of Szeged (I-74-12/2012, XI./352/2012).
The protocol were approved by the Institutional Review Board (IRB) of Dankook university dental hospital (IRB No. H-1509/008/002), and this study followed the guidelines of Helsinki Declaration.
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