Cut 75% of your prototyping costs and deliver medical devices in days, not weeks—discover how leading OEMs do it.
SHANGHAI--(BUSINESS WIRE)--NAMSA, the world’s only Medical Research Organization (MRO) that accelerates medical device development through integrated laboratory, clinical research and regulatory ...
AMES, Iowa – New research shows companies cut funding for research and development in response to a tax imposed on medical devices as part of the Affordable Care Act. R&D expenditures – $34 million ...
The Atomic Spectroscopy Group at the National Institute of Standards and Technology, which provides definitive measurements integral to developing biomedical instrumentation that helps diagnose health ...
Recognizing the increased use of artificial intelligence in the development of new therapies, the U.S. FDA on Monday released separate draft guidance on the use of the technology in the development of ...
TOLEDO, Ohio--(BUSINESS WIRE)--NAMSA®, the world’s only Medical Research Organization (MRO) that accelerates medical device development through integrated laboratory testing, clinical research and ...
On average, around 4,500 drugs and medical devices are pulled from shelves across the United States each year. 1 This alarming statistic underscores the importance of controlling and mitigating risk ...
If you’re a medical device inventor, developer, or start-up with an innovative medical device idea, choosing the perfect medical device contract manufacturer is essential to the success of your ...
This certificate program is designed to prepare biomedical engineers to understand the environment into which their innovations will be placed and the users who will interact with them. Professionals ...
Some medical technologies are just plain cool. But tech that’s only cool is never enough. It must solve specific health problems, improve each patient’s quality of care, and be easy to use. To create ...
The advent of artificial intelligence (AI) and data-driven methodologies has triggered a wave of transformation in regulatory compliance and quality assurance for the development of medical devices.