Investigative Dermatology and Venereology Research (ISSN: 2381-0858)

Description

The authors must ensure that proper protocol has been followed for conducting the clinical trials and written informed consent form should be obtained from each trial subject before initiating the trial. The IRB or ethics committee approval should be obtained and proper monitoring of the trial should be ensured. All the case studies or clinical trial reports must follow guidelines for statistical analysis and reporting of trial results (SAMPL). The authors must be willing to provide the editorial board with the informed consent form and other ethical approval forms, if required.