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Thinking About the Box: Considerations for Transport of Investigational Products
Ensure safe transport of investigational products with meticulous planning and rigorous procedures to mitigate hazards and uphold biosafety.
Building a Foundation for Regulatory Success in the Post-Pandemic Landscape
Read how an eRegulatory system can increase productivity, improve compliance, and ensure a return on your technology investment.
IRB Review of Social Media Recruitment and Retention Programs
Explore how existing regulations can establish best practices in using social media for clinical research participant recruitment.
Advarra Acquires Longboat
Advarra Acquires Longboat, a Leading Provider of Site Training, Protocol Compliance, and Patient Engagement Solutions This addition expands Advarra’s offerings that empower sites and engage patients to create...
Beginner’s Guide to Continuing Education Units (CEUs) for Clinical Research
Continuing education units (CEUs) are a great way to have a record of your ongoing professional development as required in clinical research.
How Staff Augmentation Assists with Successful Data Migration
With the goal to move active data from one system into OnCore CTMS, Advarra’s Staff Augmentation team worked with a customer’s associated hospital as it was faced with software termination.
Simple Strategies for Identifying Research Compliance Blind Spots
David Staley authored the article Simple Strategies for Identifying Research Compliance Blind Spots in Compliance Today.
Implementing eSource: A Guide for Operations and Technology Roles
Explore the transformative power of eSource in clinical research, streamlining data collection for efficiency and cost savings.
Lessons from the Trenches: Avoiding Common Legal Pitfalls in International Research
Emily Chi Fogler and Andrew Rusczek, attorneys practicing at Verrill Dana, LLP, discuss common legal issues for institutions and companies participating in international research.
Making a List, Checking It Twice… The Revised Common Rule Is Coming to Town!
Judith Carrithers and discuss a checklist of action items to consider and complete prior to the revised Common Rule compliance date.
Key Efficiencies Driven by a Clinical Trial Management System
Find out how sites can get the most value from their clinical trial management system (CTMS) to streamline operations.
Sites: The Key to Patient Centricity in Clinical Research
Learn three strategies for how site centricity can ensure trial success and a positive experience for your participants.
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