Post Market Surveillance

Mar 63 min read

The Shift From CE to UKCA

In the wake of Brexit, the replacement of the CE mark with the UKCA mark in Great Britain is a pivotal change.

Feb 143 min read

Classifying Medical Device Accessories: A Guide

In this article we'll talk about what separates medical device accessories from non-medical accessories and what to do about them

Jan 162 min read

Quality Plans in Medical Device Manufacturing

A quick overview of quality plans in medical device manufacturing and how they play a pivotal role.

Nov 28, 20232 min read

Case Studies in Post-Market Surveillance: Real-World Insights

Taking a look at some real-world case studies and the effect of Post-Market Surveillance.

Nov 2, 20233 min read

Device as a Service in Healthcare

Subscription services are everywhere, and now they're spilling into healthcare. Get ready for Device as as Service.

Oct 24, 20233 min read

Telemedicine: The Digital Doctor Will See You

Telemedicine is a game changer, but it's easy to forget that the platforms are medical devices.

Oct 18, 20234 min read

Quality Metrics for Medical Devices

Quality Metrics for medical devices are about patient safety and, literally saving lives. What are some common ones?

Oct 12, 20233 min read

The Cloud As A Medical Device

The classification of cloud platforms as medical devices are a major shift in healthcare. Let's take a look at what this actually means.

Sep 27, 20233 min read

Apps as Medical Devices

As our smartphones become more a part of us, medical device apps start to move to our phones.

Sep 20, 20233 min read

Beyond Compliance: Post-Market Surveillance Data for Product Innovation

A look at how Post-Market Surveillance should not only be used for compliance, but for innovation.

Aug 30, 20233 min read

Decoding Adverse Event Reports: Using NLP in Post-Market Surveillance

More intricate devices lead to more intricate monitoring. The ability to decode adverse event reports using NLP could be an unlock.

Aug 18, 20232 min read

Ensuring Medical Device Quality: Post-Market Clinical Follow-up Studies

In the dynamic realm of medical devices, the journey doesn't end once a device hits the market. There's a continuous cycle of learning,...

Aug 4, 20232 min read

Real-World Evidence and Post-Market Surveillance: Value for Medical Devices

A look at the value of real-world evidence in post-market surveillance and its impact on medical devices

Jul 25, 20233 min read

From Detection to Action: Streamlining Response Protocols in Post-Market Surveillance

Orchestrating a response protocol in post-market surveillance

Jul 18, 20233 min read

Integrating Social Media Feedback into Post-Market Surveillance

Social media feedback must be included in a robust post-market surveillance program.

Jun 27, 20234 min read

Artificial Intelligence (AI) and Machine Learning (ML) in Medical Devices: An Overview

Regulatory Overview of Machine Learning (ML) and Artificial Intelligence (AI) in Medical Devices.

Jun 7, 20234 min read

More Data Doesn't Always Mean Better Surveillance

More data doesn't always mean better data, or better surveillance.

May 16, 20234 min read

Unleashing Generative AI in Post-Market Surveillance: An Unlock for Medical Devices

Artificial intelligence and its potential to revolutionize post-market surveillance in the medical device industry.

Apr 25, 20233 min read

Navigating Post-Market Surveillance for Medical Devices

Post-market surveillance (PMS) is an essential aspect of ensuring the safety and efficacy of medical devices throughout their lifecycle.

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