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MedTech Intelligence

Volume 9 Issue No. 07

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


Featured Articles

Remediation: Considerations During the ProcessRemediation:
Risk Priorities

By Maria Fontanazza, Editor-in-Chief

Part III of the series on remediation looks at how companies can tie risk priorities into the remediation process.

Devine Guidance

Christopher Devine, Ph.D., Devine Guidance International Misbranded Lap Bands & Prison, What a Tale!

By Christopher Devine, Ph.D.,
Devine Guidance International

Selling expired devices? Oh, no.

Ames Gross, Pacific Bridge MedicalEstablishing a Medical Device Presence in China?
Be Very Careful

By Ames Gross, Pacific Bridge Medical

Get to know the local government, including the available benefits and incentives first.


AllerganAllergan to Buy Zeltiq Aesthetics for Nearly $2.5 Billion

By MedTech Intelligence Staff

The acquisition adds to the company’s plastic surgery and regenerative medicine portfolio.

Krish Kupathil, MobiliyaAugmented Reality for
Medical Equipment

By Krish Kupathil, Mobiliya

AR offers a seamless connection between the virtual and the real world, making it the ideal tool to be used for a range of healthcare applications, equipment and treatment procedures.


More Articles »

Sponsored Content

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about Micro-Molding

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Resource Centers

Resource Centers are single topic focused micro-sites within MedTechIntelligence.com that are portals of information on medical device components and quality systems offering news, articles, white papers, case histories and videos.

Sponsored Resources

UL - Be ready for major changes to EU Clinical EvaluationBe ready for major changes to EU Clinical Evaluation

Published in June 2016, the revised MEDDEV 2.7/1 revision 4 guidance document introduces several changes to the existing requirements for clinical evaluations of medical devices and is already being adopted by EU Notified Bodies. The revision introduces more complexity into the process that every device manufacturer selling in the EU needs to understand in order to plan and prepare.

Download this white paper “Meeting the EU’s Clinical Evaluation Requirements for Medical Devices” to find out more.

Upcoming Events & Webinars

February, 2017February 28-March 1, 2017 - Global Regulatory Strategy

Washington, DC

March, 2017March 1-2, 2017 - FDA Advisory Panels: A Workshop for Medical Device Companies

Washington, DC

March, 2017March 7-8, 2017 - Remediation of Medical Device Quality Systems

Washington, DC

March, 2017March 21-22, 2017 - Medical Device Software

Washington, DC

March, 2017March 23-24, 2017 - Medical Device Cybersecurity

Washington, DC

April, 2017March/April 2017 - Medical Device Statistics for Non-Statisticians

Washington, DC

May, 2017May 2017 - HHE and Recalls: FDA & Industry Procedures & Practices

Washington, DC

June 5-6, 2017 - China: The MedTech Market

Washington, DC

June 2017 - Combination Products: A Conference for Drug, Devide, Diagnostics, & Biologics Manufacturers

Washington, DC

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