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ICH E6(R3) Implementation Starts Now: Are You Ready?
The release of ICH E6(R3) in January 2025 marks the most significant evolution in Good Clinical Practice (GCP) guidelines in over a decade. More than a revision, E6(R3) marks a shift from traditional practices—making participant safety and data reliability not just priorities, but design drivers, and introducing risk-based proportionality as a foundational approach.
Making Just-in-Time Oncology Trials Work: Overcoming Barriers and Unlocking Potential
Making Just-in-Time Oncology Trials Work: Overcoming Barriers and Unlocking Potential As part of Oncology Research Pulse, our new thought leadership
An Interview with Jim Kremidas: What’s Next for the Association of Multisite Research Corporations (AMRC)
Launched in January 2025, the Association of Multisite Research Corporations (AMRC) was set up by its founding members to advance
Current State of Site-Sponsor-CRO Collaboration
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.
Demystifying North American IRB/EC Requirements for International Research Professionals
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Not if, but When: A Study Manager’s Guide to Adaptability and Incoming Trends
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.
Reducing Site Burden Throughout Study Startup
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
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.
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.
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.