Reducing Site Burden Throughout Study Startup
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Site
Overseeing and Operationalizing Patient Recruitment Across Study Stakeholders
This webinar will tackle the most pressing challenge in clinical research: achieving enrollment targets on time. Our presenters will investigate the recruitment lifecycle across key stages, including vendor referrals, prescreening, consent, and more. Additionally, they will examine how sponsor and CRO study teams can gain better insight into recruitment activities and to predict, analyze, and intervene appropriately.
Unlocking Global Potential: Partnering Across Varying Sites in Study Startup
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Fireside Chat: The Future of Clinical Trials and Site Engagement
Learn about the challenges sites face and see how sponsors and CROs can work more collaboratively with sites to improve study startup and address the changing clinical trial landscape.
The Ohio State eReg Case Study
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
Advantages and Considerations for an eRegulatory Implementation
Learn best practices for eRegulatory (eReg) systems, and hear tips for academic medical centers, cancer centers, and health systems.
Business Best Practices for Running a Clinical Research Site
Discover how eSource platforms revolutionize clinical trials by simplifying data collection and ensuring accuracy, accessibility, and reliability.
Participant Payments for OnCore
Simplify and streamline clinical trial participant reimbursements and stipends with Advarra Payments.
CCPay
CCPay enables clinical trial sites to streamline participant payment workflows, track payments in real time, and enhance overall financial management.
Choosing Your Electronic IRB System: A Guide for Sites
Selecting an electronic institutional review board (eIRB) system is a critical decision for institutions looking to streamline their research compliance
How Your Study’s Informed Consent Can Help Simplify Study Startup
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Clinical Research Staffing
Reduce the burden of testing and documentation with precompiled validation materials, available through an annual subscription.