The Advantages of Outsourcing IRB and IBC Reviews to One Partner
Gene therapy studies are a relatively recent addition to the world of clinical research. As a result, the unique requirements […]
Site/Sponsor Relationships
Returning to In-person Work: Sponsor Versus Site Viewpoints
As March 2020 completely disrupted any sense of normalcy, including in the workplace, many were forced to adapt rather quickly.
Op-ed: Missing Elements of the Discussion on Decentralized Trials
The discussion on decentralized clinical trials (DCTs) has been brought to the forefront in the wake of the COVID-19 pandemic.
Sites: The Key to Patient Centricity in Clinical Research
We’ve heard and used the term “patient centricity” for years now, and with good reason. It’s an important consideration in
Encouraging Site Centricity and Collaboration at Onsemble
During the week of October 5-8, more than 1,700 Advarra technology customers gathered virtually for the Fall Onsemble Conference. A
Ensuring a Successful and Collaborative SDLC Process
At Advarra, it’s our mission to ensure safer, smarter, faster clinical research every step of the way in the research
Understanding eSource, ePRO, and EDC
eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant experience, and overall study efficiency through technology integration.
The Value of Early Engagement with Your IRB
It’s no secret that in clinical research, everything moves at a quick pace – and that doesn’t stop when working
Why Institutions Should Consider an Externally Administered IBC
Clinical trials for gene therapy are booming, especially in the fields of oncology, infectious diseases, rare diseases, and regenerative medicine.
Study Activation: Top Four Takeaways from Research Sites
While enrolling subjects is arguably the most crucial aspect of clinical research operations, this cannot be done without activating a
Site-Driven Metrics: Operational Data To Improve Research
The true value of metrics is to measure operational performance in order to improve internal processes. In clinical research, this is highly beneficial when applied where the work is conducted: at the sites.
How to Successfully Conduct Virtual Investigator Meetings
In a remote clinical research landscape, a successful virtual investigator meeting can ensure a more cost-effective and compliant clinical trial.