At the 2023 Evidence Matters MedTech Roundtable, Dr. Matthew M. Cooper, Vice-President, Medical Affairs, Corporate Health & Safety at 3M Health Care, Chris Manrodt, Head of Data Strategy - IGTD at Philips, Dr. Matthias Fink, Senior Clinical Consultant at AKRA Team...
Derek Lord
Webinar Recap: Abbott Diagnostics and AKRA Team on More Confident IVD Regulatory Submissions (RAPS Western Canada Chapter event)
In a recent webinar, DistillerSR customer Dr. Victoria Samonte, Medical Director of Global Medical Operations at Abbott Diagnostics and Dr. Bassil Akra, CEO and Founder at the AKRA Team GmbH were joined by Michelle Zaharic, CEO at MLZ Biotech Consulting and IVD Lead...
Webinar Recap: ICON and Oracle Share Literature Surveillance Best Practices for Pharmacovigilance
In a recent webinar, DistillerSR customer Andrew Purchase, Director of Pharmacovigilance, UK QPPV, Site Head (Swansea, UK) at ICON was joined by Michael-Braun Boghos, Senior Director Safety Strategy at Oracle Life Science, and moderated by Peter O’Blenis, DistillerSR...
Webinar Recap: Adelphi Group and Excerpta Medica on Leveraging AI-Enabled Classifiers for Faster, More Efficient Systematic Literature Reviews
In a recent webinar, DistillerSR customers Rosie Morland, AI and Data Science Specialist at Excerpta Medica and Remon van den Broek, Head of AI Strategy and Data Science at Adelphi Group were joined by Mark Priatel, VP of Software Development at DistillerSR. They...
Systematic Reviews: Automating Your Workflows With DistillerSR
Collecting, evaluating and managing evidence is the most crucial part of research that drives policy and regulates medical technologies, and Systematic Reviews are the cornerstone of evidence-based research. A Systematic Review may contain tens of thousands of...
For the Record with Peter O’Blenis, CEO at DistillerSR
In a recent interview to Medical Alley, Peter O’Blenis, CEO at DistillerSR, discussed the company's innovation track record and the results of a recent market survey conducted with medical device and in-vitro diagnostics manufacturers, shedding light on how automation...
Webinar Recap: NuVasive and Geistlich Pharma Share Best Practices for EU MDR State of the Art Submissions While Achieving More Efficient Literature Reviews with DistillerSR
In a recent webinar, DistillerSR customers Monique Liston, Senior Medical Writer at NuVasive and Shelley Jambresic, Senior Clinical Evaluations Manager at Geistlich Pharma were joined by Dr. Bassil Akra, founder and CEO of Akra Team GmbH, Dr. Julien Senac, Global...
PRISMA Statement: Interviewing the Lead Author of the Updated PRISMA 2020 Statement on Systematic Reviews
The publication of the original PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analysis) statement in 2009 ushered in a paradigm shift in the importance of transparent reporting in systematic reviews. The statement is endorsed by several hundred...
Webinar Recap: Streamlining Health Technology Assessments by Automating Literature Reviews
At our recent webinar, we were joined by Maria Arregui, Ph.D. Assistant Director, Evidence Generation and Communications at Xcenda; Chris Waters-Banker, Ph.D. Director of Consulting Operations at Maple Health Group; Rajshree Pandey, Ph.D. Associate Director, Evidence...
ICON Q&A: How Can Automation Support Literature Surveillance for Pharmacovigilance?
Andrew Purchase, Director of Pharmacovigilance & Patient Safety and UK QPPV at ICON sat down with Vivian MacAdden, Senior Manager, Industry Marketing at DistillerSR to discuss the critical role of literature surveillance in the pharmaceutical and biotechnology...