Build HIPAA compliant software with the latest guide from Catalyst UX, a leader in UX for medical and life sciences. Whether you need to update legacy software, move to mobile or launch a new digital solution, you’ll want to read this guide. We cover what HIPAA is, who is affected, how HIPAA impacts UX design, […]
3 Tech Trends That Will Accelerate Manufacturers’ Time to Market
The medical device manufacturing market is expected to exceed $600 billion globally by 2025, but this rapid growth is accompanied by unprecedented levels of technological innovation. Read “3 Tech Trends That Will Accelerate Manufacturers’ Time to Market” to see the new advancements driving the industry and what they can offer your business. Download the trend […]
Achieving High-Resolution, Ultra-Precise Features
Precise miniature plastic parts are the result of exact tooling execution. By understanding the tolerances of both micro tooling and micro injection molding, it’s possible to achieve a high level of repeatability and part accuracy for even the most advanced micro medical devices. Download the white paper from MTD Micromolding to learn more…
Architecting for Change: Embracing a Platform Approach
How to Thrive in a Digital Era. As new innovations become more critical to business success, organizations must contend with the challenge of updating legacy technologies. “Architecting for Change: Embracing a Platform Approach” demonstrates how adopting a cloud-based quality platform allows your business to grow and adapt with the changes ahead.
Metrics that Matter for Quality Manufacturing
MasterControl Manufacturing Excellence delivers results. Life sciences manufacturers are seeing some eye-opening improvements, like 80% faster post-production review and release times. Read Metrics That Matter for Quality Manufacturing to learn how.
New EU Medical Device Regulations May Impact Your Business
The new European Union (EU) Medical Device Regulation (MDR) will impact medical device manufacturers’ product-development timelines. All companies intending to sell their devices in Europe must understand the new MDR and how it differs from the previous directives, especially in terms of new biocompatibility standard requirements. Download the white paper to learn more…
Designing Medical Devices with Multiphysics Simulation
This case study shares insights from engineers at Abbott Technologies on how they use multiphysics simulation to model left ventricular assist devices (LVADs) to improve the outlook and quality of life for patients with heart failure. Read on to learn how simulation software allowed Abbott to evaluate the structural integrity of the external controller of […]
