
In a recent interview to Medical Alley, Peter O’Blenis, CEO at DistillerSR, discussed the company's...
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Collecting, evaluating and managing evidence is the most crucial part of research that drives policy and regulates medical technologies, and...
In a recent interview to Medical Alley, Peter O’Blenis, CEO at DistillerSR, discussed the company's...
In our most recent webinar, DistillerSR customers Monique Liston, Senior Medical Writer at NuVasive...
The publication of the original PRISMA (Preferred Reporting Items for Systematic reviews and...
At our recent webinar, we were joined by Maria Arregui, Ph.D. Assistant Director, Evidence...
Andrew Purchase, Director of Pharmacovigilance & Patient Safety and UK QPPV at ICON sat down with...
At our recent webinar, we were joined by Dr. Shirley Sylvester, Therapeutic Area Medical Affairs...
In our most recent webinar, DistillerSR customers Christa Goode, Director of Clinical and Medical...
A presentation at the Medical Librarian Association’s 2021 virtual conference brought together...
One key component of realizing Evidence-informed decision making (EIDM) is ensuring decision...
Our clients screen over 50,000 references every day – over 4 million in total to date – and have...
We are currently living through an unprecedented global pandemic. All of our lives are impacted by...
Systematic reviews are a time-consuming and resource-intensive process. Even when the review is...
Although artificial intelligence technology is advancing at an incredible pace, it’s still common...
Artificial intelligence (AI) is a hot topic in the literature review world these days. For...
It’s common knowledge that “positive” results are often published more frequently and widely than...
At DistillerSR, we believe in the power of evidence-based research. As a software company, we...
One of our goals for this year was to create a user conference for DistillerSR users to come...
In general, a systematic review describes the rigorous process of systematically searching,...
Medical device manufacturers working towards EU MDR compliance are running out of time. Although...