Western Companion Diagnostic Firms Gain Foothold in the Japanese Market
This mode of personalized medicine helps doctors make more informed decisions related to drug therapies.
Tag Archives: Focus Article – Homepage
First Step in EU MDR Compliance: The Gap Analysis
A gap assessment provides a toolbox for the decision-making process.
FDA Encourages Innovation and Safety as Part of Medical Device Regulatory Overhaul
The agency’s latest announcements are indicative of its focus on risk reduction while promoting innovation.
AI-Driven Technology Reduces Risks Associated with Labor by Providing A Second Set of Eyes
It is time to extend AI’s use into labor & delivery departments, where the technology can help guide care teams to mitigate risks and make informed decisions.
2019 MedTech Predictions
Smart technologies will continue to play a big role in advancing decision-making efforts.
Amazon’s Software Service Mines Medical Records, Aims to Improve Treatment and Lower Costs
Amazon Comprehend Medical uses machine learning to pull important medical information from patient records.
Misconceptions of EU MDR Implementation
Lack of preparation and understanding of the efforts required to comply with the regulation will hinder product launches, negatively impact sales, and hurt a company’s reputation.
How to Plan for EU MDR So You Can Sleep at Night
Learn about the implications of changes to ISO 10993-1 and the introduction of the MDR, stages of pre-clinical device testing, why chemical characterization is more important than ever before, and how device manufacturers can begin assembling the right team of testing experts to ensure their products are safe and ready for market.
Augmented and Virtual Reality Make Inroads in Asia’s Medtech Market
Digital reality technologies are fast emerging as promising tools to aid physicians and patients. Western and Asian medtech companies are becoming big players in the growing market for these new applications in Asia.
FDA Commish and CDRH Director Announce Agency Actions to Enhance Patient Safety Using Data
The agency will be improving postmarket surveillance, looking at issues that come up once a device is on the market, and promoting innovation.
