Achieving EU MDR compliance is considerably challenging for many businesses, which is why they must be discerning when it comes to selecting suitable partners.
Global travel restrictions proved it impossible to hold the event in-person.
Robotic process automation (RPA) is reducing time spent on repetitive tasks in regulatory affairs and regulatory operations. The next step is artificial intelligence-enhanced RPA, which has the potential to automate more unstructured tasks.
Across Asia, government health and safety authorities have tightened regulations on medical devices this year, as markets continue to experience rapid change, and as the devices themselves gain sophistication and complexity at a blistering pace.
A Q&A with MedCrypt’s Axel Wirth sheds light on urgent problems that the medtech industry is facing regarding device security, but assures us that the sky is not falling.
Combining “fit, filtration and efficiency” is the key to enhancing protection and encouraging compliance.
Leveraging automation and data analytics can help facilitate innovation and financial stability.
Medical device recalls were up more than 31% during Q2 2020, activity that suggests recalls will reach 1200 by the end of the year, according to Stericycle’s latest recall report.
Managing how a material can affect a device’s success starts with a strong, collaborative relationship with your materials supplier, which can help prevent a myriad of issues throughout the development of medical devices.
Devices in healthcare facilities support mission critical processes. Any issue that degrades network performance can have serious consequences.
