Soapbox

What MedTech Product Business Owners Must Know About Private Investments

By John Geis, Cresset Partners

For founders and owners of privately held medical product businesses, the amount of private investment dollars available is significant.

MedTech Deals Worth
$15.8 Billion in Q2

By MedTech Intelligence Staff

Overall activity in deals jumped 11% in North America.

FDA Monitoring Potential Device Shortage After Atlanta Sterigenics Facility Temporarily Closes

By MedTech Intelligence Staff

Will more medical devices be impacted?

Start-up Trends at MEDICA

By Messe Düsseldorf

The transition to digital in healthcare is happening at a fast pace.

Featured Quote

Full public access to all adverse event reports enables innovation, leads to better, safer medical devices, and benefits the patient, caregiver and device maker.

— Jesse Ambrosina, Ivenix

App Alerts Patients and Caregivers to Medical Device Recalls

By MedTech Intelligence Staff

Scan a barcode for access to important product instructions, safety and recall information.

MEDdesign

Medical Wearable Sensor and Software Platform Driving Healthcare Applications in Remote Patient Monitoring

By Jiang Li, Ph.D., VivaLNK

To remove the barriers to RPM solutions, we need to empower application developers.

Do you have a product design and need manufacturing support?

The first step is to make sure your design is ready for manufacturing. When designing a plastic part many design factors need examined. Crescent Industries’ white paper uncovers some of these design concerns and how to overcome them. If you need help, a good injection molder will provide feedback and discuss these issues with you. These steps ensure your part/device meets the requirements for manufacturing and functionality. Read our white paper now!

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

Medical Device Cybersecurity:

Legacy Device Remediation, Compensating Control & End-of-Life Conference, September 26-27, 2019

Plan to attend this Workshop at the Medical Device Interoperability & Cybersecurity Lab at MGH, Boston, MA or "virtually" from your own location via a webcast.

This highly interactive program is intended to help manufacturers and hospitals – independently and in collaboration – better understand steps they can take to improve medical device cybersecurity throughout the product life cycle.

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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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