Breakout Session III
Dive deeper into specific topics in these focused and interactive discussions.
Assessing Feasibility Of Site Structure Standardization
Standardizing site and site network structures can enhance operational efficiency, quality assurance, and regulatory compliance across clinical research sites. Benefits and challenges of standardization will be discussed, as well as feasibility assessments. Join us to examine case studies and discuss strategies for achieving consistency and excellence in site management and performance.
Embracing Diversity & Inclusion In Research
Embracing diversity and inclusion is vital for enhancing trial representation across diverse populations, improving patient engagement, and meeting regulatory requirements. Gain insights into promoting equity, diversity, and inclusion (EDI) initiatives that elevate research quality while ensuring ethical standards and compliance.
Navigating Budget Negotiations With Inflation
This forward-thinking session will discuss how to navigate your budget negotiations in response to current inflationary pressures. Learn how to adapt your financial frameworks, nurture partnerships, and optimize negotiations to achieve mutually beneficial outcomes amidst economic challenges.
Supporting Sites Through Technology Implementation & Challenges (ENCORE)
Solutions at your service! This session will explore how clinical research technology implementation and troubleshooting support can empower research sites. Discuss practical solutions aimed at enhancing site operations, overcoming common challenges, and ensuring smooth study execution.
The Impact Of CTIS On Research Workflows
This session will assess the impact of the Clinical Trials Information System (CTIS) on clinical research workflows. Analyze the functionalities, benefits, and potential challenges of CTIS implementation on regulatory processes, transparency, and efficiency. Ensure your site is fully equipped for the transformative implications of CTIS within the clinical research landscape.