Sponsors
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.
FDA Update: BIMO – What Sponsors Need to Know
This webinar highlights key changes to the compliance program and provides recommended best practices for inspection readiness programs.
Reflections from Cell and Gene Meeting on the Mesa 2021
This blog recounts the 2021 Cell and Gene Meeting on the Mesa conference, including details on cell and gene therapy's growth and trajectory.
Advarra Announces SiteIQ™ to Optimize Clinical Trial Feasibility
SiteIQ leverages IRB & other data sets to provide unique analysis across experience, capacity, quality, performance, & patient eligibility.
Steps to Implementing a Quality Management System
Read our blog to learn more about quality, its role in clinical research, and how to implement a management plan.
Advarra Trend Report: The Future of Work in Clinical Research
Download our report to learn more how the COVID-19 pandemic impacted the future of the clinical research workforce.
Video: Introduction to Data Monitoring Committees
More studies now require oversight than ever. DMCs are required when a trusted independent third party is necessary to assess clinical trials
Clinical Research Staffing Reprioritizations and Resourcing Strategies
Gain insights on how to work through staffing reprioritizations and options to consider when planning resourcing strategies.
Navigating the Ethics of Remote Research Data Collection
In this article, Luke Gelinas develops a framework to identify and address key challenges for remote research data collection.
When do I Need a DMC?
View our infographic to learn the basics of a data monitoring committee (DMC), also referred to as data safety monitoring board (DSMB).
The Importance of Keeping DSMBs Independent
By ensuring the DSMB is truly independent from study conduct, sponsors make trial data more trustworthy and enhance public confidence.
Introduction to Advarra Consulting
Our experts work directly with your team to accelerate product development & performance, making clinical research safer, smarter, and faster.
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