Informed eConsent Forms – Revolutionizing Clinical Trial Administration
eBook
This comprehensive eBook explores the next generation of eConsent—from digital platforms and multimedia enhancements to the ethical use of AI in clinical trials. Learn how RWS helps sponsors streamline processes, improve patient comprehension, and meet global compliance standards.
Key topics include:
- The role of AI in eConsent and translation
- Enhancing patient engagement through plain language
- Meeting EU and FDA expectations for lay summaries
- Building inclusive, multilingual consent strategies
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