Stephen Hahn to be Named FDA Commissioner,
says President Trump

By MedTech Intelligence Staff

The White House issued a statement on the president’s intent to nominate Hahn, who is currently the chief medical executive at The University of Texas MD Anderson Cancer Center in Houston.

Stephen Hahn, MD
(Photo: The University
of Texas MD Anderson
Cancer Center)

Reimagining Eye Care
in Asia

By Mary Kan and William Greene, Singapore Biodesign

The future of eye care will sit at the intersection of the digital and physical worlds.

Satisfying the Market’s Growing Appetite for
Product Data

By Frits Stulp

Iperion Life Sciences Consultancy

Whatever the demands of international regulators, it is public expectations that will ultimately dictate the need for life sciences companies to prepare complete and accurate product data that patients and healthcare providers can scrutinize on demand.

Understanding Skin and Designing Wearable Devices

By Patrick J. Parks, M.D. Ph.D.,
3M Health Care Business Group

Skin is an ever-changing organ.

Featured Quote

Medical product business owners should not only look for the right partner to invests in their companies, but ideally one that can also help them preserve their newfound wealth and nurture its growth.

— John Geis, Cresset Partners

Stryker to Acquire Wright Medical for $4 Billion, Will There Be Antitrust Issues?

By MedTech Intelligence Staff

The deal is expected to close in the second half of 2020, but one analyst expects the transaction will raise antitrust issues in the United States.

Soapbox

Where MedTech Is Going in the Next Decade, An Irish Perspective

By Rachel Shelly, IDA Ireland

Medtech decision makers must accurately predict future trends in order to chart the best future directions and identify the most advantageous areas for business investment.

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

EU MDR: REQUIREMENTS & IMPLEMENTATION

THIS EVENT WAS RECORDED JULY 17, 2019 | On Demand Webcast

This on-demand recording of the four-hour virtual event that took place July 17, 2019, conducted by leading experts on EU MDR requirements and implementation, provides concise insights into key aspects of the regulation to help companies understand and plan for the impending changes. The four hour webcast recording is $495.00

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ADVANCED CAPA & ROOT CAUSE ANALYSIS

THIS EVENT WAS RECORDED MARCH 26-27, 2019

CAPA is the most critical and challenging quality system requirement in terms of complex thinking and organizational processes. How do you verify effectiveness? How can you apply project management to CAPA? What are the right data and tools for identifying trends? How do you deal with significant but infrequent problems? Should you set deadlines for closing CAPAs, and what about CAPAs that never close? What are best practices for documenting and communicating CAPA results? Not a CAPA 101 course, this workshop recording brings together leading industry CAPA process owners to discuss approaches to the most difficult problems in CAPA and root cause analysis.

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