#5

Soapbox

Supplier Quality Considerations For Quality and Regulatory Service Providers

By Bryan Brosseau,
Brosseau Consulting, LLC

When outsourcing these key functions, asking the right questions will help minimize the risk.

#4

Why Paper-Based Systems
No Longer Make the Cut

By Alex Condon, Galen Data;
Chris Byers, Formstack; and
David DeRam, Greenlight Guru

Here’s what these three CEOs think about why the transition to digital is more important than ever.

#3

Corrections, Corrective Actions, and Preventive Actions:
Effectively Handling Nonconformances in Compliance with the EU MDR

By Bryan Brosseau, Brosseau Consulting, LLC

An explanation of these principles and the actions that must be addressed in compliance with 21 CFR 820, ISO 13485 and the EU MDR.

#2

Soapbox

Three Hospital Trends Impacting Medtech Manufacturers

By Patrick Vega, Vega Healthcare

How manufacturers can better understand their customers in a rapidly changing provider environment.

#1

EU MDR Cost of Compliance:
The Results Are In

By Maria Fontanazza, Editor-in-Chief

Here's what companies think when it comes to how much it will cost to comply with the new regulation.

Skin should be a critical part of your device development process.

[VIDEO] Learn what skin means to Jacquie & Milena

Designing devices for skin requires a skin-first approach. Watch the video and download this complimentary report to find out why.

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