MedTech Intelligence Volume 9 Issue 07

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	Volume 9 Issue No. 07

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

Featured Articles

Remediation: Considerations During the Process Remediation:
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 Medical Establishing 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.

Featured Quote

By using human factors engineering in combination with design psychology, what should be an intimidating and stressful procedure becomes something quite the opposite.

— Niall Redmond, Starfish Medical

Allergan 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, Mobiliya Augmented 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.

Sponsored Content

5 Things Everyone Should Know
about Micro-Molding

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Pacific Bridge Medical - Sourcing in China: Best Practices for Medical Device Companies

FDA Advisory Panels - February 28 - March 1, 2017 - Washington, DC

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

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

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.

Medical Device Audits, Certification & Verification
sponsored by SGS
Quality & Regulatory Market Access Solutions
sponsored by UL
Medical Device Component
sponsored by 3M

Sponsored Resources

UL - Be ready for major changes to EU Clinical Evaluation Be 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 28-March 1, 2017 - Global Regulatory Strategy