# Regulations in Clinical Trials

IRB Submission Strategies in the United States and the European Union

Clinical Trial Management

The process of submitting participant materials to Institutional Review Boards (IRBs) in the United States and Ethics Committees (ECs) in the European Union is a […]

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The process of submitting participant materials to Institutional Review Boards (IRBs) in the United States and Ethics Committees (ECs) in the European Union is a

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Joseph Farrell

December 9, 2023

ESIGN and eIDAS: Understand eConsent Regulations in Clinical Trials

Regulatory Compliance

eConsent has become a critical component in clinical trials, offering improvements in efficiency, data quality, comprehension, and patient engagement. Two key regulations governing electronic transactions

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eConsent has become a critical component in clinical trials, offering improvements in efficiency, data quality, comprehension, and patient engagement. Two key regulations governing electronic transactions

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Joseph Farrell

October 19, 2023

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