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More than 60 percent of clinical studies submitted to CDER contain data from foreign study sites.
Researchers need to be aware of the cultural differences, legal and regulatory requirements — and international guidelines — dictating principles for obtaining informed consent.
Get prepared to adapt global informed consent templates to local country requirements.
This management report will help trial sponsors and investigators navigate the international informed consent landscape with practical advice about:
Order Obtaining Consent in International Clinical Research today to get prepared for conducting international clinical trials.
Order Your Copy Today!
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