The Impact of Public Perception of Clinical Research
Undoubtedly one of the biggest news stories around the world during the past year has been the one surrounding the
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To Be Patient-centric, Be Site-centric
Patient centricity has long been a key goal in healthcare, as well as in clinical research. Sponsors want their participants
Research Site Dramatically Increases Funding through Advarra’s Budget Negotiation Service
Learn how Advarra’s Budget Negotiation Service helped a site increase funding by 260%, reduce costs, and achieve faster study turnaround times.
Top 10 Pharma Achieves Enrollment Across 600 Sites
Download the case study to see how Advarra Enroll increased ease and efficiency for site prescreening, while providing sponsor teams essential visibility into recruitment progress.
How Staff Augmentation Assists with Successful Data Migration
Staff Augmentation aids data migration by assessing workflows, ensuring a smooth transition to OnCore, and empowering teams with tailored training.
Top 20 Pharma Accelerates Training and Improves Compliance Across 650 Site Staff Trial
Advarra’s Study Startup solution provided training for every staff member at every global trial site, inclusive of real-time training reports, helping to ensure all 20,000 patients enrolled were treated exactly according to protocol, and enrolled seven months ahead of target
Top 10 Educational Resources of 2020
It’s safe to say 2020 has been more unpredictable than anyone could imagine. Through these unprecedented times, we have worked to provide the
Top 20 Biopharma Doubles Recruitment and Reduces Screen Failures Across 188 Sites
Top 20 Biopharma Doubles Recruitment and Reduces Screen Failures Across 188 Sites A top-20 pharmaceutical company conducted a complex Phase
Top 30 Biopharma Activates and Enrolls Across 164 Sites
In this case study learn how Advarra Study Startup and Advarra Enroll helped a top-30 pharmaceutical company achieve study startup milestones on time while setting their sites up for recruitment success.
Beginner’s Guide to Investigator-Initiated Trials
While many clinical trials are initiated by industry sponsors, such as pharmaceutical companies or contract research organizations (CROs), other trials
Q&A – The Must-Haves of FDA and Common Rule Reporting Requirements
In a recent webinar, Advarra regulatory experts discussed the must-haves of FDA and Common Rule reporting requirements. They reviewed the basics of what must be reported to whom—and when—for sponsors and investigators involved in IND studies, as well as requirements for identifying, reviewing, and reporting unanticipated problems and noncompliance to IRBs and Common Rule departments or agencies. Due to time constraints we weren’t able to answer all audience questions during the Q&A period, so our experts have answered some of the most popular questions in this blog.
Getting “Engaged” in the Time of COVID
When using remote sites to perform clinical trial procedures, there are certain issues researchers must keep in mind, including whether those remote sites are considered to be engaged in research.