Overcoming the Challenges of Medical Device Complaint Handling with AI: How 3Analytics Leads the Way
The medical device industry plays a pivotal role in global healthcare, deliveri [...]
18
12, 2024
5
12, 2024
AI in Medical Device Manufacturing: How It’s Transforming an Industry
In April 2018, the U.S. Food and Drug Administration (FDA) approved the first A [...]
30
05, 2023
Complaint Management for Life Sciences with an Automated QMS
Effective complaint handling is fundamental to life sciences quality management [...]
25
04, 2023
Update: EU Medical Device Regulation Deadlines Extended
European Union (EU) Medical Device Regulation (MDR) and In-Vitro Device Regulati [...]
29
11, 2022
How Hybrid Audits Can Help MDR Compliance in the European Union
The shortage of notified bodies (NB) in the European Union is a key challenge fo [...]
25
08, 2022
EU MDR & IVDR Regulation: Where Does the Guidance Stand?
Companies marketing devices in the European Union are facing a perfect storm of [...]
30
06, 2022
EUDAMED Update: What You Need to Know Now
The European Union (EU) Medical Device Regulation (MDR) officially went into eff [...]
17
02, 2021
Remote Audits in the Age of COVID-19
Amid the ongoing pandemic, groups like the European Commission (EC) and the Inte [...]
15
02, 2021
AssurX Webinar – EU MDR Preparedness: Implementing a MIR-Ready Complaint Management Solution
Join us for a one-hour webinar focused on efficient management of postmarket cha [...]
21
01, 2021
EU MDR Countdown: What’s Next for Medical Device Compliance
In four months, the new EU Medical Device Regulation (MDR) goes into effect, whi [...]
