Advarra is excited to introduce Fireside Chats, a series of virtual conversations discussing current issues in clinical trials. Each Fireside Chat brings together perspectives from across the research community, enabling real-time discussion of contemporary challenges and potential solutions to help make research altogether better.
You likely have short-term projects to be completed quickly, or large ongoing projects delayed due to a lack of time and resources. We can assist with both.
The global pandemic has changed the way we think about research. Sponsors should consider how the “new normal” will impact sites and current studies as they plan to re-start research.
On Clinical Trials Day, now more than ever, it’s important to recognize and thank those unsung heroes at the focal point of research: research sites and institutions.
Now more than ever, people are seeking out employment at organizations that offer more than just standard benefits. They are
Research doesn’t just inform medical treatment; it informs public health and public policy, and it helps explain human behaviors.
Independent verification of compliance opens new doors for CRIO, Inc. and provides customers confidence that they can incorporate the eSource system into their own computer software validation strategy.
Advarra Consulting provides in-depth analysis of German, European, and US regulations, allowing a cancer research study to move forward.
As we near the end of 2019, let’s take a look back at the blogs that generated the most interest this year from readers like you.
Site timelines for studies can vary widely across the industry due to differences in internal efficiency. In this blog, James Riddle (Advarra VP of Institutional Services and Strategic Consulting) tells the tale of two sites, one with an integrated research administration, and one without.
Discover strategies to fortify your research administration program, from setting a new vision to supporting QA/QI initiatives.
When does a quality improvement program cross over into research? How do the two categories inform one another in the context of human subjects protection? Advarra IRB Executive Chair Sarah Harnish clarifies the divisions on these two related, but separate categories.
