Key Barriers to RWD Adoption

By MedTech Intelligence Staff

A new survey from Frost & Sullivan highlights the key barriers to adoption of real world data and analytics in health care and life sciences.

Registration Opens for March IMDRF Meeting in Washington, DC

By MedTech Intelligence Staff

The 25th session of the International Medical Device Regulators Forum will be held March 11-15 in Washington, DC. The free event is open to the public and includes both in-person and virtual attendance options, Registration deadline is February 16.

Top 5 Safety Hazards in Medical Device Manufacturing
(and How to Reduce the Risk)

By Steven John Cumper, MedShop

Manufacturing jobs can be dangerous, but knowledge is the first step to minimizing the risks associated with these positions. This article discusses five of the most common safety hazards in medical device manufacturing, with tips on how to reduce the risk of employee injuries while maintaining productivity.

Makatsaria Takes Helm as CEO of LivaNova

By MedTech Intelligence Staff

Vladimir A. Makatsaria, who most recently served as Company Group Chairman at Johnson & Johnson MedTech, leading its global Ethicon surgery business, has been appointed CEO of global medical technology company LivaNova. Former CEO Bill Kozy will serve a Board Chair.

Navigating Global Regulations for SaMD

By Dhaval Shah, CitiusTech

Decoding the legal framework for faster time-to-market.

Featured Quote

AI has transcended conventional boundaries, offering a new understanding of breast cancer’s complexities. Its impact is felt not only in laboratories and hospitals, but throughout the healthcare system.

— Ted M. Diehl and Wayne Brinster, PreciseDx

How redesign can help meet sustainability demands
for medical devices

Redesign using Design for Environment principles can help medtech companies meet sustainability demands for their devices. See how to analyze and use eco-smart designs that account for sustainable materials, product durability, and improved energy efficiency.

Download to learn more

The ultimate guide to the EU MDR and IVDR GSPR, 2nd Edition

5 eSTAR Challenges MedTech Regulatory Teams Must Overcome

How to Achieve Optimal Weighing Performance with Lab Balances

Better device outcomes through better data

The Emergence of Lateral Flow Assays in Diagnostics

Terumo Enables Global Collaboration and Clinical Excellence for Groundbreaking Medtech Research

Drive Healthcare Transformation with Enterprise-Level Infrastructure

2023 MedTech Regulatory Performance Report