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Electronic Informed Consent (eIC): How The FDA/OHRP Final Guidance Affects You
Sandra “SAM” Sather
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Electronic Informed Consent: New Guidance-Implications and Implementation
Betsy Fallen
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ICH GCP E6 (R2) Refresher Training Bundle
Sandra “SAM” Sather
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Monitoring Informed Consent (IC): Frequently Asked Questions
Sandra “SAM” Sather
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Pediatric Clinical Trials: Special Considerations and Requirements
Chuck Sather
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Quality Risk Management Post ICH GCP E6 R2 Addendum
Sandra “SAM” Sather
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