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Home ›  Best Practices

The Informed Consent Process for Clinical Trials and Research – Best Practices Across Countries

  • By: Staff Editor
  • Date: September 30, 2011
Webinar All Access Pass Subscription 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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