December 9, 2025 – 11:00 AM ET
Join CRIO and a panel of industry experts for a balanced discussion on one of the most debated questions in clinical operations: Should sponsors provide standardized, study-specific source document templates to investigative sites?
This webinar will explore the operational, legal, and regulatory considerations behind the issue, highlighting both the advantages and risks of template standardization. Attendees will walk away with greater clarity on why the industry remains divided—and what guidance, requirements, and best practices exist today.
Key themes include:
• Why the question is so debated
• Benefits of sponsor-provided templates
• Compliance concerns and operational risks
• Regulatory and legal interpretations
• How stakeholders can move toward greater confidence
Speakers: Doug Schantz (Asklepios BioPharmaceutical), Edye Edens (EDEE Law), Dr. James Clark (Alcanza), Melissa Gottschlich (ICON)
Moderator: Raymond Nomizu, Co-CEO, CRIO