The responsible conduct of basic and clinical research Andrzej Górski Introduction To The Proceedings Of The 6th International Bioethics Conference Held In Warsaw, Poland, 3–4 June 2005 Pages: 3 - 4
The physician’s role in the protection of human research subjects John R. Williams OriginalPaper Pages: 5 - 12
Managing data for integrity: Policies and procedures for ensuring the accuracy and quality of the data in the laboratory Chris B. Pascal OriginalPaper Pages: 23 - 39
Fostering integrity in research: Definitions, current knowledge, and future directions Nicholas H. Steneck OriginalPaper Pages: 53 - 74
The concept of risk and responsible conduct of research Eugenijus Gefenas OriginalPaper Pages: 75 - 83
Some methodological aspects of ethics committees’ expertise: The Ukrainian example Svitlana V. Pustovit OriginalPaper Pages: 85 - 94
The mentor and the trainee in academic clinical medicine Tadeusz S. Tołłoczko OriginalPaper Pages: 95 - 102
The definition of adequate care in externally sponsored clinical trials: The terminological controversy about the concept “standard of care” Hans-Jörg Ehni OriginalPaper Pages: 123 - 130
The protection of patients’ rights in clinical trials Marek Czarkowski OriginalPaper Pages: 131 - 138
Evaluation of drug toxicity in clinical trials Jacek SpławińskiJerzy KuźniarWaldemar Zieliński OriginalPaper Pages: 139 - 145
The poehlman case: running away from the truth John E. DahlbergChristian C. Mahler OriginalPaper Pages: 157 - 173
Biomedical research and mining of the poor: The need for their exclusion R. R. Kishore OriginalPaper Pages: 175 - 183
Conference summary: ‘The responsible conduct of basic and clinical research’ Raymond E. Spier OriginalPaper Pages: 189 - 197