Volume 11 Issue No. 20
Who’s Responsible for Securing IoT Medical Devices?
By Christopher Morales, Vectra
Long-term industry efforts are essential in closing the gaps in the device ecosystem.
Choosing The Right QMS For Your Medical Device Company
By Evan Luxon, Centese
Going paperless is easier than you think.
Harmonization of medical device regulations allows the medical device industry to focus on unified set of regulatory requirements to comply with, thus reducing costs and increasing efficiencies. The new 510(k) process is a move in the right direction.
— Jay Mansour, EAS Consulting Group, LLC
MedTech Engineers:The Next Generation
By Mark Keene, Ph.D., Metrasens
The future of medical technology is dependent on current engineering students and their mentors.
Growth in Medical Devices Spurs Recruitment Challenges
By Luke Moran, Aerotek
In addition, in workforce optimization, retention plays an equally important role as recruitment.
More Articles »
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.
May 20-21, 2019 - EU MDR Supply Chain & Economic OperatorsA Virtual Conference
May 21-22, 2019 - EU MDR Clinical & Postmarket Surveillance StrategiesA Virtual Conference
May 23-24, 2019 - EU MDR Labeling, IFU, UDI, & EudamedA Virtual Conference
October 22-23, 2019 - Global Regulatory StrategyWashington, DC
October 23-24, 2019 - MedTech M&A: Regulatory & Quality Due DiligenceWashington, DC
November 13-14, 2019 - India - the MedTech Market: Strategic Planning & Practical ConsiderationsWashington, DC