How to Improve Your Site Compliance
In this ebook we discuss Break down the most common site violations, and reasons for protocol deviation and Discuss tactics and strategies to help your site team overcome these common challenges.
Professional Services
Optimizing Site Initiation Timelines Through Centralized Processes
A centralized CTMS team streamlines trial initiation by uniting resources, ensuring data accuracy, and reducing bottlenecks for efficient site startup.
Trend Report: DE&I in Clinical Research: Where we are Today
Explore the state of DE&I in clinical research with survey insights on diversity plans, budgeting efforts, and progress in trial representation.
Addressing Industry Challenges: Staff Turnover
Staff turnover in clinical research impacts trial quality and timelines. Addressing this requires focus on workplace culture, career growth, and competitive benefits.
Turbocharging Clinical Trial Activation Timelines
Streamlining clinical trial activation requires balancing budgets, approvals, and feasibility—all while accelerating timelines to meet key goals.
Children’s Hospital Expedites Study Process with Advarra’s Professional Services
Discover how Advarra helped a children’s hospital overcome staffing shortages, optimize budget negotiations, and improve efficiency.
Clinical Trial Startup: Insights from the Industry
The clinical trial startup process has seen significant shifts over the past five years: growth in decentralized trials, improved technology,
Unlocking Study Activation: 2023 Study Activation Report
Discover how evolving tools and processes affect study activation and learn strategies to reduce delays and administrative burdens in research.
Public Perceptions of Clinical Trials: A Comprehensive Survey
The clinical research industry is only becoming more complex and competitive as organizations are inundated with multiple trials and tight
New and Emerging CMS Policies: Medicaid’s New Clinical Trial Policy
The Centers for Medicare & Medicaid Services (CMS) released a letter outlining routine costs in clinical trials for patients eligible
Ace Your Next FDA Inspection
Adhering to FDA guidelines is crucial for sponsors and sites to ensure successful inspections, enabling product approvals and faster market access.
4 Unique Challenges of Oncology Trials
Oncology trials face unique hurdles in innovation, enrollment, and endpoints, requiring strategic planning to address complex study demands and precision needs.