Let's Talk Risk!
Let's Talk Risk! with Dr. Naveen Agarwal
RM roundup #2: 10 noteworthy risk-related LinkedIn posts
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RM roundup #2: 10 noteworthy risk-related LinkedIn posts

A reading of highlights from 10 noteworthy risk-related posts recently published on LinkedIn. Links to each original post and their authors are listed in notes below.

Listen to my reading of a recent LinkedIn article I published to cover 10 noteworthy risk-related posts recently published on LinkedIn. Listen to the recording and follow links below to read the original posts and continue the conversation.


🗞️A roundup of 10 noteworthy risk-related posts on LinkedIn!


1️⃣ Randy Horton spotlights top 10 Health Technology Hazards for 2024 compiled by ECRI.


2️⃣ Marco Felsberger reminds us that planning is useful, but building capability is even more important to handle uncertainty in our complex world.


3️⃣ Chad Johnson explains how using a QFD can help us focus on the customer when building an FMEA


4️⃣ Mark F. Witcher, Ph.D. encourages us to take a systems-view of risk instead of an event-based view during risk analysis.


5️⃣ Boris Gurevich shares a draft document from IMDRF on SaMD device considerations and risk characterization.


6️⃣ Darrin Carlson, RAC-Devices, PMP highlights the omission of DHF, DMR and DHR from the QMSR and how to map them under ISO 13485.


7️⃣ Jan Beger shares a study that focuses on factors affecting patients' trust in AI for treatment decisions.


8️⃣ Joseph Kvedar shares a review article about risk prediction models using AI for diabetes care and unresolved issues for implementation.


9️⃣ Stefan Hunziker, PhD, CICP highlights an unintended consequence of ignoring correlation among individual risks.


🔟Annmarie Nicolson shows how HFE activities interact with multiple workstreams during design and development.


Share in comments 👇your favorite risk-related post covered in this podcast.

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Discussion about this podcast

Let's Talk Risk!
Let's Talk Risk! with Dr. Naveen Agarwal
Every Friday, Dr. Naveen Agarwal leads a Let's Talk Risk! conversation with industry colleagues to discuss practical challenges and share best practices in risk management. In the highly regulated world of medical devices, most practitioners struggle with the "how" of risk management. Regulatory requirements are complex, confusing and ever changing. Establishing an effective risk management process that satisfies the scrutiny of regulators and auditors without creating barriers to innovation is a significant challenge in the industry. Dr. Agarwal believes that no single "expert" has all the answers, and it is only when we connect, share and learn from each other that we all become better. Let us keep learning together!