From Hesitation To Confidence: Should Sponsors Provide Source Document Templates To Sites? Let's Debate

The question of whether sponsors should provide source document templates to investigative sites is far from settled—and the implications are significant. This on-demand webinar brings together expert perspectives to unpack the operational, regulatory, and compliance considerations behind this debate. Attendees will explore why hesitation exists, what benefits standardization could deliver, and where caution is warranted.

Key themes include the case for sponsor-provided templates, potential risks and compliance uncertainties, and the influence of global regulatory frameworks on decision-making. Through structured discussion, participants will gain clarity on unresolved questions, such as whether templates compromise site autonomy or enhance data integrity.

If you’re navigating clinical trial documentation strategies, this session offers practical insights to help you weigh both sides of the argument and move toward informed confidence.

Watch now to understand the legal realities, operational trade-offs, and strategic considerations shaping this critical industry conversation.