MEDdesign

Why Software-Powered Electronics Manufacturing is Advancing the Medtech Industry

By Sudeep Goswani, Tempo Automation

Software-powered PCBAs can help medical device engineers generate high-quality prototypes for complex electronics products in record speed.

Zimmer Biomet Gets FDA Nod for First Pediatric Spinal Tether Device

By MedTech Intelligence Staff

The agency granted its first approval order under the humanitarian device exemption in spinal pediatrics in the last 15 years.

Advanced Wound Care Market Expected to Surpass $22 Billion by 2030

By MedTech Intelligence Staff

The aging population and the rising rate of diabetes globally are fueling market growth.

Featured Quote

The shift from in-hospital to remote patient care is opening up the competitive landscape and allowing smaller, more agile and innovative companies to create novel solutions.

— Jiang Li, Ph.D.

MEDdesign

How One Medtech Manufacturer Used Barcode Software to Up Its Efficiency Game

By Nick Recht, TEKLYNX International

By simplifying labeling compliance, companies can focus on better serving current and new markets.

Event Reports Virtual Workshop Targets Non-Conformances and CAPAs

By MedTech Intelligence Staff

This two-part workshop will help participants understand how to better use data from non-conformances as well as how to effectively communicate issues.

Soapbox

EU MDR: Changing World
of Classification

By Peter Rose, Maetrics

Class I device manufacturers need to keep on top of new classification rules to avoid loss of market share under the close approaching EU MDR deadline.

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.

More Info