New Industry Framework Targets Repetitive Clinical Trial Site Training
Site-Sponsor Consortium Releases Practical Recommendations and Tools to Reduce Duplication, Ease Site Burden, and...
2026 Trend Report
Reducing Avoidable Protocol Amendments by Anticipating Operational Pitfalls Hidden in Clinical Trial Design
Protocol amendments are a costly but common part of clinical trials, often reflecting gaps between scientific ambition and real-world execution.
News
Advarra Launches Site Identification Technology with Insights Directly from Sites
New capability pairs intelligence from Advarra’s robust IRB and site source-of-truth operational systems, giving...
PRIM&R Launches Educational Initiative to Advance Ethical AI Governance in Research with Grant from Advarra
New programming will equip research oversight professionals with independent education, leadership dialogue, and practical...
Advarra’s Study Design Solution Named “Best Clinical Study Design Solution” in 2026 MedTech Breakthrough Awards Program
Landmark 10th annual awards program, which received over 5,000 entries, recognizes the most innovative digital health and medical technology solutions worldwide COLUMBIA, Md., – May 7,...
Blogs
5 Warning Signs Your Study Startup Workflow Needs Attention
Study startup depends on coordinated work across sponsors, contract research organizations (CROs), sites, review...
When Are Adaptive Designs Best Suited for Oncology Trials?
Adaptive study designs are best suited for oncology clinical trials when meaningful uncertainty exists...
Why We Funded AI Ethics Education for Research Oversight —and Left the Agenda to PRIM&R
As AI becomes part of research workflows, the people responsible for ethical oversight need...
Types of Audits in Clinical Trials
Clinical trial audits are independent quality assurance evaluations of trial activities, records, systems, facilities,...
Webinars
Meeting Sites Where They Are: A Connected, Intelligence-Powered Operating Model
Meeting Sites Where They Are: A Connected, Intelligence-Powered Operating Model This on-demand webinar, presented...
Ensuring Operational Feasibility in Next-Generation Oncology Trials
Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing...
Embedding AI And Critical IRB Operations Data To Drive Intelligent Study Design
Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing...
Enabling Oncology Site Success: Overcoming Administrative and Operational Barriers to Advance Cancer Research
Enabling Oncology Site Success: Overcoming Administrative and Operational Barriers to Advance Cancer Research Oncology...
Featured Resources
EDC Companion Paper: Reducing Redundant Site Training Through Competency-Based, Role-Based, and Reusable Training Models
Recognition, evidence, vendors, and pilots Supported tools This companion paper is paired with Tool...
SIV Companion Paper: Reducing Redundant Site Training Through Competency-Based, Role-Based, and Reusable Training Models
Placement, reuse, and live discussion design Supported tools This companion paper is paired with...
Reducing Redundant Site Training Through Competency-Based, Role-Based, and Reusable Training Models
Main framework paper for site training reform, SIV redesign, and EDC recognition Developed by...
Operationalizing Responsible Artificial Intelligence (AI) in Clinical Research
Executive Summary Artificial intelligence (AI) is rapidly becoming embedded across the clinical development lifecycle,...