Research Compliance
Budgeting and Billing Compliance in Study Activation
From making do with a tight budget to taking less conventional approaches, learn how you can ensure that reliable timelines are maintained.
Increase Recruitment, Retention, and Compliance with Engaging Site Training
In this webinar, learn how site training can impact your study’s success from recruitment, retention, and compliance.
Beginner’s Guide to Connected Clinical Research Ecosystems
Learn about technologies and services that help conduct efficient and collaborative clinical trials in a connected research ecosystem.
Beginner’s Guide to Compliant Electronic Source Data Capture
Learn about electronic source data capture in clinical trials, relevant regulations, and best practices.
VERO Biotech Gains FDA Approval for Complex Drug and Device Combination
Learn more about how VERO Biotech leveraged Advarra Consulting to successfully navigate the pathway to FDA approval
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.
Understanding International Data Transfer’s Impact
Read our blog to understand some of the data privacy implications facing international clinical research.
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.
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.
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.
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