MedTech Event: EU MDR Updates and Evidence Management Best Practices
NuVasive
NuVasive streamlined literature reviews for more efficient CER submissions with DistillerSR.
Geistlich Pharma
Geistlich Pharma completes literature review screening 85% faster than manual methods using DistillerSR.
Philips
Philips achieves faster, more accurate literature reviews for CER submissions with DistillerSR.
Case Study
Dr. Bonnie H. Weiner describes the way DistillerSR reduced the time it took to complete CER literature reviews by approximately 30%.
Case Study
DistillerSR enabled faster, more efficient literature reviews, while improving collaboration amongst a distributed global workforce of medical writers.
Abbott Diagnostics
DistillerSR Enabled the Abbott Diagnostics Team to Complete Literature Reviews 50% Faster
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.
Market Survey
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.
Linkedin Live
What the EU MDR Compliance Extension Really means to Medical Device/IVD Manufacturers
Webinar
Automation and Literature Review Software Adoption Driving More Confident Regulatory Submissions
Webinar
MedTech Summit US 2022 Roundtable: Best Practices for Streamlining Literature Reviews for Post-Market Surveillance (PMS)
Webinar
Literature Review Strategies & Best Practices While Establishing State of the Art for EU MDR Compliance
Webinar
Literature Review Strategies for Post-Market Surveillance – A Best Practices Webinar
Webinar
From Manual to Automated Literature Reviews for CER & PER Submissions: A Faster Path to Compliance
Webinar
Are You Reg. Ready? Getting Your Medical Affairs Team Primed to Manage New Regulatory Requirements
Webinar
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.
Blog
Q&A Blog Post: How Can Automation Support Literature Surveillance for Pharma and Biotechnology?
Blog
Ian Stefanison, CTO for DistillerSR, answers questions on how AI reprioritization reduces screening times by as much as 80%, according to one study.
Blog
NuVasive and Geistlich Pharma Share Best Practices for EU MDR State of the Art Submissions While Achieving More Efficient Literature Reviews with DistillerSR
Video
Automating Literature Reviews for Pharmacovigilance Animated Video
Recording
Pharmacovigilance Mistakes Are Not an Option: Literature Reviews and Pharmacovigilance