STRATEGIES FOR MANAGING TRIAL REGISTRATION REQUIREMENTS COMPLIANTLY AND EFFICIENTLY

Disclosing clinical trial information in public registries is a complex process. When individual trials require registration in multiple public registries, the process becomes convoluted. This practical webinar will present strategies for managing trial registration requirements compliantly and efficiently, including:

• Writing the all-important SOP for registering trials in public databases
• Addressing the numerous deadlines associated with trial registration
• Facing the challenge of disclosing text consistently across multiple public databases

Speaker:
Joyce Swart
Senior Manager of Clinical Trial Disclosure
Alcon Research Inc., a Novartis Company

Contact:

Brooke Akins | Division Director, Life Science Programs
+1 (312) 224-1693 | bakins@q1productions.com​