Medical Device Professionals Use DistillerSR
For Audit-Ready, Compliant CER & PER Literature Reviews 

Learn why four of the top five global medical device companies trust DistillerSR to automate CER & PER literature reviews in an efficient, audit-ready, and compliant way.

Related Resources

Medtech Summit Europe 2022 Customer Conversations


Customer Chat with Geistlich Pharma

We caught up with Shelley Jambresic, Senior Clinical Evaluation Manager at Geistlich Pharma on how DistillerSR helps her complete literature reviews 50% faster.

Watch Video
Criterion Edge

Customer Chat with Criterion Edge

We caught up with Laurie Mitchell, President at Criterion Edge on her longtime journey with DistillerSR and how it helps her complete literature reviews efficiently, accurately and faster. 

Watch Video

Medtech Summit Europe 2022 Recap

Day 1 Recap

Day 1 Recap

Marc Dufresne, VP of Strategic Growth and Duane Leitch, Senior Director of Professional Services at Evidence Partners sum up the first day at MedTech Summit Europe 2022.


Watch Video
Day 2 Recap

Day 2  Recap

A special feature with Peter O'Blenis, CEO at Evidence Partners and Bassil Akra, CEO & Founder AKRA Team GmbH discussing current challenges for medical device manufacturers facing EU MDR and IVDR compliance.


Watch Video

Final Recap Recording

Marc Dufresne, VP of Strategic Growth and Duane Leitch, Senior Director of Professional Services at Evidence Partners recap the week at MedTech Summit Europe 2022. 



Watch Video
Philips Case Study-2

Case Study

Philips achieves faster, more accurate literature reviews for CER submissions with DistillerSR.

Read the Case Study
ABM Brief Mockup

Business Brief

Automated literature reviews provide greater levels of auditability and program management to CER and PER submissions.


Read the Brief
PMS Brief-1

Business Brief

Literature review best practices help accelerate EU-MDR post-market surveillance (PMS.)


Read the Brief

Getting Started with DistillerSR

We take a holistic approach to making you successful. From configuring your first project to advising on a complex research protocol, to training your team and answering support questions, we are here to ensure you are successful from day one. So what do our customers think about our approach? They have given us a 92% customer satisfaction rating.


The clinical evaluation team at Philips cut down title and abstract screening by 74%, full text screening by 70%, and flowcharts/diagrams creation by 50%.

Sara Garbin, Senior Clinical Development Scientist at Philips

No video selected

Select a video type in the sidebar.

Book a Demo