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Are the Votes of Ethics Committees in Germany for the Protection of Clinical Study Trial Subjects “Sovereign Acts?”

‚Mirroring‘ the Ethics of Biobanking: What Analysis of Consent Documents Can Tell Us?

Overcoming Language Barriers in the Informed Consent Process: Regulatory and Compliance Issues with the Use of the “Short Form”

P. M. Lad and Dahl, R., Overcoming Language Barriers in the Informed Consent Process: Regulatory and Compliance Issues with the Use of the “Short Form”, Accountability in Research: Policies & Quality Assurance, vol. 21, no. 5, pp. 315-320, 2014.

The Ottawa statement on the ethical design and conduct of cluster randomized trials: A short report

Identifying Gaps in Suicide Research: A Scoping Review of Ethical Challenges and Proposed Recommendations. (Cover story)

Shaping Medical Students' Attitudes Toward Ethically Important Aspects of Clinical Research: Results of a Randomized, Controlled Educational Intervention

Community Hospital Oversight of Clinical Investigators' Financial Relationships

Research Participant Safety and Systems Factors in General Clinical Research Centers

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