Research Operations
Adapting, Adopting, and Succeeding in a Decentralized Landscape
Join a discussion on the exponential evolution of clinical trials, uncover trends observed across the industry, and hear how leading research organizations have adapted to a decentralized landscape.
FDA Communications Through the Drug Development Lifecycle
Understand how to effectively communicate and build a relationship with the FDA throughout the drug development lifecycle.
CCText Empowers Critical Two-Way Communications for Eurofins CR
Download the case study to learn how Eurofins leveraged CCText to enhance the patient experience and improve efficiency.
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.
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