2025: Perspectives and Predictions From Advarra Thought Leaders
2024 has been a year of growth and evolution in clinical research. The coming year is expected to be no […]
Research Operations
Choosing Your Electronic IRB System: A Guide for Sites
Selecting an electronic institutional review board (eIRB) system is a critical decision for institutions looking to streamline their research compliance
The Importance of a Large Network of KOLs for DMCs
In the complex landscape of clinical trials, the data monitoring committee (DMC) serves as the cornerstone at the intersection of
The Power of Worldwide Networks in Data and Safety Monitoring Boards
In an era where clinical trials are increasingly global, it’s more imperative than ever to leverage international expertise. Data and
Budgeting and Contracting Best Practices for Research Sites
To grow your business, negotiate and collect fair payment for your work by understanding its true costs before budget discussions.
The Evolution of Clinical Quality: Key Considerations from ICH E6 R3
The International Council for Harmonisation (ICH) good clinical practice (GCP) guidelines are critical in ensuring the safety and rights of
Bacteriophage Therapy: A Promising Solution to Antibiotic Resistance
Antibiotic resistance is an emerging problem. Some have argued bacteria are developing antibiotic resistance faster than we can research, develop,
Strategies For Efficient Clinical Trial Budget Management
Managing clinical trial budgets efficiently is necessary for the success and sustainability of clinical research sites. Effective budget management not
Budgeting for IRB Review: A Guide for HRPP Leadership
At institutional research programs around the U.S., there exists a pervasive myth: internal institutional review board (IRB) reviews are free.
Understanding the Impact of the New EU Artificial Intelligence Act on Clinical Research
Artificial intelligence (AI) has taken the world by storm – and regulators are paying attention. The European Parliament recently adopted
Good Manufacturing Practices: When Do They Apply?
Navigating cGMP application in investigational drugs can be complex. Learn how FDA guidelines help clinical teams maintain safety and quality from early trials to commercialization.
Developing a Data-driven Feasibility Process
Clinical research is complex and resource-intensive, and to understand just how far an organization’s resources can go, assessing a study’s