MAPS EMEA 2025
Featured Resources
Purpose-built GenAI for Literature Reviews
Learn how reviewers can focus on high-value work, reduce fatigue, and meet the rising demand for faster, more accurate reviews.
Scientifically Validated AI
DistillerSR is a pioneer in the use of AI for literature reviews.
Webinar
Data Harmonization Driving Trusted Evidence Management Throughout the Product Life Cycle
Additional Resources
Boston Scientific
Boston Scientific Accelerated Regulatory Submissions by Transforming Literature Review Processes With DistillerSR
Stryker
Stryker improves literature evidence management efficiency by 70% with DistillerSR.
NuVasive
NuVasive streamlined literature reviews for more efficient CER submissions with DistillerSR.
Abbott Diagnostics
DistillerSR enabled the Abbott Diagnostics team to complete literature reviews 50% faster.
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.
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
Blog
Xcenda, Maple Health Group and Curta discuss how automating literature reviews helps streamline HTAs submissions.
Medlior
With as many as 40,000 references per project, Medlior, used DistillerSR to more accurately and efficiently manage their literature reviews.
Maple Health Group
DistillerSR enabled Maple Health Group to improve efficiency and optimize resource allocation.
Webinar
Automation and Literature Review Software Adoption Driving Confident IVDR Regulatory Submissions
Webinar
Leveraging Data Reuse for More Efficient Evidence Management Throughout the Medical Device Lifecycle
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
Recording
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
Streamlining Health Technology Assessments (HTAs) by Automating Literature Reviews
Webinar
Literature Review Strategies for Post-Market Surveillance – A Best Practices Webinar
Webinar
How Literature Review Automation and Efficient Processes Streamline RWE HEOR Studies
Webinar
Are You Reg. Ready? Getting Your Medical Affairs Team Primed to Manage New Regulatory Requirements
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.
Webinar
Stay Ahead Of The Game: How To Conduct An Evidence-Based GVD Faster And Smarter To Improve Market Access
Webinar
Streamlining Health Technology Assessments (HTAs) by Automating Literature Reviews
Webinar
How Literature Review Automation and Efficient Processes Streamline RWE HEOR Studies
Webinar
Can Literature Review Automation Improve Healthcare Cost-Effectiveness Analysis and Budget Impact Modeling Outcomes?
Webinar
How Information Overload is Driving New Approaches for HEOR Systematic Literature Reviews
Webinar
Data Harmonization Driving Trusted Evidence Management Throughout the Product Life Cycle
Improve Cost-Effectiveness Analysis and Budget Impact Modeling Using Literature Review Automation Software
This business brief outlines a customized SLR solution for health economics and outcomes research.
Real-World Evidence: Using Systematic Literature Reviews for Evidence Synthesis…
A guide for researchers using systematic reviews for RWE study design or RWE literature synthesis.
Information Overload Drives New Approaches to Managing HEOR Literature Reviews
Apply automation and intelligent workflows to HEOR literature reviews to improve health decisions.
Streamlining Health Technology Assessments by Automating Literature Reviews
Automating some of the functions of a review can increase the efficiency and accuracy of HTAs.
Smart Automation of SLRs for GVDs: Faster Market Access for New Drugs
Automating aspects of the SLR can improve its accuracy and efficiency while supporting the development of a…
Enterprise Evidence Management for Trusted Healthcare Decision Making
Discover how an enterprise evidence management strategy can lead to product success and better patient outcomes.
Future-Proofing Evidence for Better Patient Outcomes
Product data, be it from preclinical development, bench testing, clinical studies, real-world evidence (RWE), or scientific literature reviews…
Purpose-built GenAI for Literature Reviews
Learn how reviewers can focus on high-value work, reduce fatigue, and meet the rising demand for faster, more accurate reviews.
HEOR & HTA Fact Sheet
Automate and simplify the management of researchers’ systematic collection of secondary data.