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MedTech Intelligence

Volume 10 Issue No. 44

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

Devine Guidance

Christopher Devine, Ph.D., Devine Guidance International Failure to Protect Patient Data is a Crime

By Dr. Christopher Joseph Devine, Devine Guidance International

All employees who handle patient information must be appropriately trained to HIPAA.

Featured Articles

Maria Fontanazza, Editor-in-ChiefM&A: Once the Deal Closes, What Should I Do?

By Maria Fontanazza, Editor-in-Chief

Look for the good, the bad, and the ugly, but above all, look for anything that affects patient safety.

Infographic: RAdiation ScienceRadiation Science:
Breakthroughs That Change Lives

By Sarah Daren, Freelance Writer

An infographic that shows advanced tools making imaging safer and more effective.

EU MDR Compliance CostWhat is the Cost of Compliance with EU MDR?
Take the Survey

By MedTech Intelligence Staff

Be a part of the conversation. Results of the survey will be revealed next week!

MEDICA Preview


Dr. Lutz Retzlaff, Contributing WriterHow Start-Ups Are Trying to Conquer the Market

By Dr. Lutz Retzlaff, Freelance Journalist

Early-stage companies are seeking cures for diseases from heart conditions to skin cancer.


Horst Giesen, Messe DüsseldorfDigitization and IT Trends Among Key Topics at

By Horst Giesen, Messe Düsseldorf

Digital transformation, artificial intelligence and start-up technologies are some of the topics that will be discussed at the event in Germany this month.

MEDICAMEDICA to Showcase Trends
in Interconnected Health and Mobile Aid

By Dr. Lutz Retzlaff

From intelligent prosthetics embedded with sensors to cuff-less blood pressure monitoring to smart patches, wearable technology continues to make leaps and bounds.

Sponsored Content

Crescent Industries4 Things You Need to Know about FDA Registered Manufacturers

FDA registration is a mechanism for notifying the FDA that a given facility is involved in the production and distribution of medical devices. Medical device contract manufacturers who register their facilities with the FDA play an important role in ensuring safety, performance, and quality of the device that benefit patients’ lives every day. To learn about FDA registered manufacturers and how Crescent Industries is an engineering-driven, technology-based injection molder for OEMs, click here.


More Articles »


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

Upcoming Events & Webinars

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

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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