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. |
Featured Articles |
MedTech Deals Worth 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? |
By Messe Düsseldorf The transition to digital in healthcare is happening at a fast pace. |
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Featured Quote — Jesse Ambrosina, Ivenix |
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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 By Jiang Li, Ph.D., VivaLNK To remove the barriers to RPM solutions, we need to empower application developers. |
Sponsored Content |
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! |
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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 |
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. |
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 |
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. |
Upcoming Events & Webinars |
September 26-27, 2019 - Medical Device Cybersecurity October 23 & 24, 2019 - MedTech M&A November 6-8, 2019 - EU MDR Implementation Strategies |
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