Balancing Innovation, Ethics, and Operational Excellence in Adaptive Oncology Trials Clinical trials are evolving to incorporate adaptive designs, offering flexibility […]
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even the most efficient teams off track. Advarra and industry representatives will dive deeper into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.
Advarra Single Sign-On (SSO) for user authentication allows users to access all SSO-enabled Advarra products in one place using just one set of credentials.
The future of study startup gives sites flexibility, while ensuring total visibility for study teams like yours. Optimize operations across each unique site, with guided configurations to ensure compliance and control.
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
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.
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
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.
Streamline participant payments with automated workflows that simplify stipends, reimbursements, and tracking for coordinators, participants, and finance teams.
