Evidence Partners Incorporated - Evidence Matters '21

MedTech Intelligence

Volume 13 Issue No. 38


Peter O‘Blenis, CEO of Evidence PartnersEU MDR Compliance:
Do Your CERs and PERs Hit the Regulatory Bar?

By Maria Fontanazza, Editor-in-Chief

MedTech Intelligence recently sat down with Peter O‘Blenis, CEO of Evidence Partners to discuss challenges reviewers face throughout their literature review process in the context of regulatory compliance, and to talk about the upcoming virtual event, Evidence Matters 2021.



SalesforceModernizing Your MedTech Selling Process

Recorded: August 4, 2021 - Sponsored by Salesforce

“COVID only helped set the wind in our sails”, said Michael Allen, AVP of Sales and Service, Dynarex, when asked about the impact of COVID to his business processes. During this On-Demand Webinar, you will be able to listen and learn how Dynarex, a medtech company was able to increase sales by improving deal time to addressing revenue leakage.

Watch Now!

Featured Articles


From Facility to Home:
COVID-19 and New Connected Health Use Cases

By Jennifer Kent, Ph.D., Parks Associates

As the focal point of care moves away from the facility and into the home, care providers and health systems will lean more heavily on connected health devices in advancing and expanding the future of healthcare.


Medical Systems Cybersecurity

By Eric C. Cosman, OIT Concepts, LLC

It’s important to draw on experience from other sectors.

DNV - Introduction to EU 2017/745 Medical Device Regulation (MDR) training - Nov 15-17


Addressing Hidden Risks in Medical Device Labeling Operations

By Chris Heckert, Network Packaging Partners and Warren Stacey, PRISYM ID

Due to rapidly evolving regulatory landscape and manufacturing demands, label requirements and the information they contain are constantly changing. Here’s how medtech organizations can manage the process.

Modalities, Timelines & Tips:
What Manufacturers Need to Know About Tissue Sterilization Validation

By John Neville, Ph.D., WuXi AppTec Medical Device Testing

The FDA requires medical device manufacturers to demonstrate the sterility of their products. Whether a device functions in vivo or in vitro, sterility is crucial to ensuring patient safety and maximizing device functionality.


Seizing the Customer Experience Opportunity in Life SciencesWhitepaper:
Seizing the Customer Experience Opportunity in Life Sciences

Salesforce and Harvard Business Review (HBR) have teamed up to dive deep on why improving customer experience is top of mind for life science organizations in “Seizing the Customer Experience Opportunity in Life Sciences” whitepaper.


Medical Instrument Sterilization Post-Pandemic:
Four Factors to Consider

By Devin Partida, ReHack

The COVID-19 pandemic has changed hospital processes and made people more aware of the need to thoroughly sterilize medical instruments between patients. This article discusses some of the changes that may occur due to lessons learned throughout the global health emergency.

Experlogix - Build Your Custom Equipment and Quotes with 100% Accuracy

MedTech Library

Datasheet: Reduce Your Medical Device Time-to-Market with CPQ SoftwareReduce Your Medical Device Time-to-Market with CPQ Software

Sponsored By Experlogix CPQ

Specifically designed for the medical device and mobility industry, Experlogix CPQ will also help accelerate the quoting and proposal generation process, empowering your sales reps to configure complex product and service proposals quickly and accurately with ease.

Top 6 uses for video on medical device assembly lines

Sponsored By Drishti Technologies, Inc.

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