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The Informed Consent Process for Clinical Trials and Research – Best Practices Across Countries
- By: Staff Editor
- Date: September 29, 2011
Abstract:The informed consent is process is a cornerstone in the ethical conduct of clinical trials and research on human subjects. Regulatory requirements for this important process varies from country to country.
This article gives an overview of best practices for getting informed consent from human subjects in various international jurisdictions.
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