Adjusting business models will help Medtech companies find ways to stay profitable in the push toward value-based care as provider needs change.
Even though plastic is easy to use, cost effective, and well established, medtech engineers can run into challenges.
Your design may not be a breakthrough, but could it help you break free from some regulatory burden?
Exploring the current state of robotic-assisted surgery and what to expect from future surgical robots.
Ernst & Young’s new Pulse of the Industry study stresses that medical device companies need to begin investing more in digital capabilities or long-term growth could be at risk.
An R&D expert will share tips for getting a product to market quickly without letting project stress drive a wedge between you and your co-workers.
Presenters at MD&M Minneapolis will discuss how using technologies from other industries can make medical device manufacturing more efficient.
Appreciate the promise of digital health technology as well as the challenges faced when launching a product, advises an expert speaking at MD&M Minneapolis.
Audrey Turley, of Nelson Labs, will speak at Medical Design & Manufacturing Minneapolis about biocompatibility issues related to medical devices including the move to more in vitro testing and the 2020 deadline for the new European Medical Device Regulation.
A study shows that standard identifiers can create efficiencies and improve accuracy in medical device order-to-cash and rebate/chargeback processes.
In fields such as biotechnology and medical devices, where ideas and projects are often the product of extensive research and collaboration across various disciplines, inventorship choices can be intricate, sensitive, and complex.