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- DistillerSR Enables Sixfold Increase in Literature Review Completion
- DistillerSR is a “Game Changer” for Medlior’s Management of Large Systematic Reviews
- DistillerSR Reduces Clinical Evaluation Report Time by 30%
- Learn How the Leading Provider of Commercialization Services to the Life Sciences Industry Leveraged DistillerSR Automation to Achieve Faster and Smarter Systematic Reviews
- Geistlich Pharma DistillerSR Case Study
- Global CRO Reduces Literature Reviews Times by 30 percent with DistillerSR
- Health Agency Uses AI to Reduce COVID-19 Citation Screening and Data Extraction By 50%
- Philips Achieves Faster, More Accurate Literature Reviews for CER Submissions with DistillerSR
- NuVasive Streamlined Literature Reviews for More Efficient CER Submissions with DistillerSR
- Philips Achieves Faster, More Accurate Literature Reviews for CER Submissions with DistillerSR
- University of Florida Conducts Reviews Faster with DistillerSR
- University of Guelph Cuts Screening Time by Almost 50% with DistillerSR AI
- Guides and White papers
- 5 Best Practices for Optimizing Your Systematic Reviews E-Book
- Buyer’s Guide to Systematic Review Software
- EU MDR State of the Art - Best Practices and Literature Review Using DistillerSR
- Smart Automation of SLRs for GVDs: Faster Market Access for New Drugs
- HEOR Fact Sheet
- Hierarchical Data Extraction Form
- How Literature Review Automation Improves CER and PER Program Management
- Improve Cost-Effectiveness Analysis and Budget Impact Modeling Using Literature Review Automation Software
- Information Overload Drives New Approaches to Managing HEOR Literature Reviews
- Literature Review Best Practices Accelerate EU-MDR Post-Market Surveillance (PMS)
- Medical Device Fact Sheet DistillerSR
- Pharmacovigilance Fact Sheet DistillerSR
- Real-World Evidence: Using Systematic Literature Review for Evidence Synthesis and Study Design Planning for Pharmaceuticals, Medical Devices, and Diagnostics
- Research Team Fact Sheet DistillerSR
- Streamlining Health Technology Assessments by Automating Literature Reviews
- The Buyer's Guide to Literature Review Software
- The Case for Artificial Intelligence in Systematic Reviews
- The Role of Literature Reviews in Establishing State of the Art (SOTA) for EU MDR Compliance
- Streamlining Health Technology Assessments (HTA) by Automating Literature Reviews
- Medical Devices Literature Review
- Brief Review of Post-Market Surveillance Activities
- Clinical Evaluation Versus Clinical Investigation
- Does the FDA Require a Clinical Evaluation Report
- EU MDR Requirements
- How Do You Write a Clinical Evaluation Plan?
- FDA Post-Market Medical Device Surveillance
- How Do You Write a Clinical Evaluation Report
- How Often Should a CER Be Updated?
- How Do You Conduct Post-Marketing Surveillance?
- IVDR Classification Guidance
- IVDR Versus IVDD
- What Are Clinical Evaluation Reports?
- How Is a PMCF Study Different From a Clinical Investigation?
- What Does a CER Contain
- What Does a Clinical Evaluation Consist Of
- What Is a Clinical Evaluation
- How Often Is a PSUR Submitted?
- What Is a Clinical Evaluation Plan
- What Is a Clinical Investigation
- What Is the Difference Between MDR and IVDR
- How to Write a Periodic Safety Update Report
- How Do You Write a Literature Review for Clinical Research
- What Is the EU MDR?
- What Is the Main Purpose of the MDR?
- What Is the Purpose of a Clinical Evaluation Report
- Periodic Safety Update Report Format
- Who Writes a Clinical Evaluation Report
- Why Is Clinical Evaluation Important?
- Case Studies