Medical Device Process Validation: A Virtual Conference - January 29-30, 2019

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MedTech Intelligence

Volume 10 Issue No. 47

Business Analysis Combination Products Market Access Operations Product Development Quality/Regulatory

Manufacturing 101Manufacturing 101: What is Metal 3-D Printing?

By Matt Sand, 3DEO

Advanced manufacturing technology in the here and now.

Featured Articles

The following stories have been the most popular articles on MedTech Intelligence this fall. One thing is clear: Readers continue to crave any content that will help them learn more about the EU Medical Device Regulation.

Autumn Top 5



Bryan Brosseau, Brosseau Consulting, LLCSupplier 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.


Why Paper-Based Systems No Longer Make the Cut 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.


Corrections, Corrective Actions, and Preventive ActionsCorrections, 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.



Three Hospital Trends Impacting Medtech ManufacturersThree Hospital Trends Impacting Medtech Manufacturers

By Patrick Vega, Vega Healthcare

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


EU MDR Compliance CostEU 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.

Sponsored Content

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More Articles »


Sponsored Resources

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Upcoming Events & Webinars

Nov. 2018November 27-28, 2018 - EU MDR Implementation Strategies Workshop
Washington, DC

December 2018December 5, 2018 - 12pm EST - Neurotechnology: Advancing Beyond Expectations
Complimentary Webinar

JanuaryJanuary 23-24, 2019 - Advanced CAPA and Root Cause Analysis Workshop for Medical Device Companies
Washington, DC

JanuaryJanuary 29-30, 2019 - Medical Device Process Validation
A Virtual Conference

February 5-6, 2019 - EU MDR Remediation Strategy
Washington, DC

February 6-7, 2019 - EU MDR Clinical & Postmarket Surveillance Strategies
Washington, DC

March 5-6, 2019 - Med Tech Import/Export
Washington, DC

March 7-8, 2019 - EU MDR Supply Chain & Economic Operators
Washington, DC

April 11-12, 2019 - EU IVDR Implementation
Washington, DC

May 7-8, 2019 - Medical Device Cybersecurity: Legacy Device Remediation, Compensating Controls, & End-of-Life
Cambridge, MA

May 21-22, 2019 - Medical Device Recalls: Current Topics & New Initiatives
Washington, DC

May 23-24, 2019 - EU MDR Labeling, IFU, UDI, & Eudamed
Washington, DC

June, 2019 - Global Regulatory Strategy
Washington, DC

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