Research Operations
ReadyQMS Info Sheet
Advarra ReadyQMS, a quality management system for biopharmaceutical companies, reduces risk and ensures regulatory compliance.
Data Integrity – It’s All About the Data!
This blog dives into data integrity in clinical research, including how to obtain and maintain data throughout its lifecycle.
Leveraging Data to Lead and Manage the Research Mission: Data-Driven Decision Making at all Levels of the Organization
This webinar discusses how an organization uses data at all levels to lead and drive the research enterprise and day-to-day operations.
6 Tips for Creating Effective Clinical Trial Training
This blog offers practical tips for effective site training to ensure your global clinical trials are compliant and efficient.
Ensuring a Successful and Collaborative SDLC Process
Find out how Advarra's approach to the SDLC lifecycle leads to successful collaborations among sites and sponsors.
US Medical Device Regulation 101
Speed the review process by understanding how medical devices are classified & what the IRB must review to approve device research.
4 Questions to Ask CTMS Vendors
Here are four questions to ask during the selection process to offer more insight into your future success with the selected vendor.
Durham Nephrology Associates Enhances Reporting and Patient Experience Using CCPay
Learn how Durham Nephrology Associates implemented Advarra CCPay to enhance their clinical trial staff and patient payment process experience.
IRB Review of Phase I Research: Balancing Ethics and Efficiency
Find out how to address Phase I research challenges to enable efficient IRB review and timely study startup.
3 Must-Haves to Deploy Remote Clinical Trials
Ensure your organization has the tools to both efficiently and compliantly implement remote modalities to best reap the benefits of DCT
Understanding eSource, ePRO, and EDC
eSource, ePRO, and EDC are integral to efficient clinical research. This blog explores how they work together and their differences.
Beginner’s Guide to Minimal Risk Research
How can researchers know when research is minimal risk? Learn an overview and the regulatory flexibilities that might be eligible.
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