Author:
Bernabe Rosemarie D. L. C.
Publisher
Springer International Publishing
Reference27 articles.
1. Al-Shahi, R., C. Vousden, and C. Warlow. 2005. Bias from requiring explicit consent from all participants in observational research: Prospective, population based study. BMJ 331: 942.
2. Aven, T. 2008. Risk analysis: Assessing uncertainties beyond expected values and probabilities. Chichester: Wiley.
3. Baron, J. 2008. Thinking and deciding, 4th ed. Cambridge: Cambridge University Press.
4. Bernabe, R.D., G.J. van Thiel, J.A. Raaijmakers, and J.J. van Delden. 2009. The need to explicate the ethical evaluation tools to avoid ethical inflation. The American Journal of Bioethics 9(11): 56–58.
5. Bernabe, R.D., G.J. van Thiel, J.A. Raaijmakers, and J.J. van Delden. 2011a. Is informed consent necessary for randomized phase IV “observational” drug studies? Drug Discovery Today 16(17–18): 751–754.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献