Medtech Summit Resources
NuVasive streamlined literature reviews for more efficient CER submissions with DistillerSR.
Geistlich Pharma completes literature review screening 85% faster than manual methods using DistillerSR.
Philips achieves faster, more accurate literature reviews for CER submissions with DistillerSR.
Dr. Bonnie H. Weiner describes the way DistillerSR reduced the time it took to complete CER literature reviews by approximately 30%.
DistillerSR enabled faster, more efficient literature reviews, while improving collaboration amongst a distributed global workforce of medical writers.
SOTA Webinar Recap
NuVasive and Geistlich Pharma Share Best Practices for EU MDR SOTA Submissions While Achieving More Efficient Literature Reviews with DistillerSR.
PMS Webinar Recap
Johnson & Johnson and Philips on their journey to streamline post-market surveillance literature reviews for EU MDR/IVDR submissions.
Dual Screening in Your Systematic Review: Is it Worth the Time?
New evidence reinforces the value of dual screening, and why you need a process to mitigate the risk of using only one screener.
Industry Survey: Literature Review Automation Adoption Insights and Trends
Literature Review Best Practices Accelerate EU-MDR Post-Market Surveillance (PMS)
Best-practices that can help streamline processes and ensure compliant EU-MDR literature reviews.
How Literature Review Automation Improves CER and PER Program Management
Automated literature reviews provide greater levels of auditability and program management to CER and PER submissions.
The Role of Literature Reviews in Establishing State of the Art (SOTA) for EU MDR Compliance
Automation can greatly enhance the success of SOTA literature reviews.
Medical Devices Fact Sheet
Used by four of the top five medical device companies in the world, DistillerSR automates the management of CER literature reviews.
What the EU MDR Compliance Extension Really means to Medical Device/IVD Manufacturers
Automation and Literature Review Software Adoption Driving More Confident Regulatory Submissions
MedTech Summit US 2022 Roundtable: Best Practices for Streamlining Literature Reviews for Post-Market Surveillance (PMS)
Literature Review Strategies & Best Practices While Establishing State of the Art for EU MDR Compliance
Literature Review Strategies for Post-Market Surveillance – A Best Practices Webinar
From Manual to Automated Literature Reviews for CER & PER Submissions: A Faster Path to Compliance
Are You Reg. Ready? Getting Your Medical Affairs Team Primed to Manage New Regulatory Requirements
MedTech Intelligence – EU IVDR Innovation in Practice: Clinical Evidence and Surveillance
Pharmacovigilance Fact Sheet
Learn how PV specialists can use DistillerSR to automate literature surveillance and reporting that’s audit-ready and compliant.
Q&A Blog Post: How Can Automation Support Literature Surveillance for Pharma and Biotechnology?
Ian Stefanison, CTO for DistillerSR, answers questions on how AI reprioritization reduces screening times by as much as 80%, according to one study.
NuVasive and Geistlich Pharma Share Best Practices for EU MDR State of the Art Submissions While Achieving More Efficient Literature Reviews with DistillerSR
Automating Literature Reviews for Pharmacovigilance Animated Video
Pharmacovigilance Mistakes Are Not an Option: Literature Reviews and Pharmacovigilance