| pubmed-article:16121655 | pubmed:abstractText | The main task of the ethics committees is the protection of study participants against unethical research. The international consensus on ethical aspects, however, is only partially considered in legal regulations. In Germany, the regulations for approval procedures of clinical studies have been increasingly standardised, but this does not apply to information for study participants. The aim of this study was to propose a list of criteria for information for study participants based on comparisons of existing resources and international standards. | lld:pubmed |
