Podcast Index
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Daily Cyber Threat Brief
Simply Cyber Media Group
MetroNews Hotline
MetroNews
AI Fire Daily
AIFire.co
9to5Mac Daily
9to5Mac
De Grote Tech Show | BNR
BNR Nieuwsradio
Behind the Numbers
Restaurant365
The Bitcoin Way Podcast
The Bitcoin Way
Raise the Line
Osmosis from Elsevier
Double Tap
Double Tap Productions Inc.
Cyber Crime Junkies
Cyber Crime Junkies. Host David Mauro.
Accès au Marché Mondial des Dispositifs Médicaux
Pure Global
Глобальный доступ на рынок медицинских изделий
Pure Global
चिकित्सा उपकरण वैश्विक बाजार पहुंच
Pure Global
Tıbbi Cihazlar Küresel Pazar Erişimi
Pure Global
Akses Pasar Global Alat Kesehatan
Pure Global
Cybersecurity Tech Brief By HackerNoon
HackerNoon
Programming Tech Brief By HackerNoon
HackerNoon
Crypto News Daily
brief.news
Gaming Tech Brief By HackerNoon
HackerNoon
AI News Daily
brief.news
Discover Crypto
HIT Network
Tech News Daily
brief.news
Primary Technology
Stephen Robles and Jason Aten
Game Mess Mornings
Giant Bomb
TED-Ed
TED-Ed
The Cyber Threat Perspective
SecurIT360
Talk of the Week
Liam
Future of Life Institute Podcast
Future of Life Institute
Einundzwanzig, der Bitcoin Podcast
Einundzwanzig
The AllinCrypto Podcast
AllinCrypto
The Med Device Cyber Podcast
Blue Goat Cyber
Reflections
Livewire Labs
Roz & Mocha
Frequency Podcast Network
LG Pro Cast: The Place for Hot HVAC Topics & Cool Conversations
LG Air Conditioning Technologies
Looks Like New
MEDLab
Proof of Law
Quantum Lex
Technologie
Blue Goat Cyber
For years, cybersecurity has been viewed as an IT responsibility. Today's threat landscape demands something very different.In this episode of the Med Device Cyber Podcast, Christian Espinosa is joined by Melissa Aarskau...
Cancer treatment is already difficult enough without adding more hospital visits, more testing, and more delays. Yet many cancer therapies carry a significant risk of damaging the heart, forcing patients to undergo regul...
When you develop a groundbreaking medical device, you assume the engineering and clinical data will carry you across the finish line. The legal landscape of U.S. market entry involves layers of corporate traps that most ...
When you try to communicate cybersecurity risks to medical device manufacturers, do you feel like you are speaking ancient Hieroglyphics? You are not alone. In this episode of the Med Device Cyber Podcast, Christian and ...
Philippe Gerwill manages to be a board advisor for nearly 30 companies without losing his humanity. In this episode of the Med Device Cyber Podcast, Christian Espinosa sits down with the world-renowned futurist to discus...
Medical software is still underestimated by teams that think generic engineering habits will carry over cleanly into a regulated environment. They do not. The work gets harder when requirements, traceability, security, t...
Early-stage MedTech gets riskier when investors confuse a compelling story with a credible device. Stronger diligence starts by testing whether the science is real, whether clinicians would actually use the product, and ...
A device can clear regulatory hurdles and still struggle commercially if the evidence is too narrow. MedTech companies need proof that speaks to affordability, care quality, operational impact, and long term value, not j...
Product decisions made during early development determine commercialization outcomes years later. Wrong choices about regulatory pathways, feature sets, and market segments create compounding problems limiting commercial...
Vibe coding enables rapid development through AI-generated code but introduces security risks when developers accept outputs without verification. Malicious actors can inject vulnerabilities through manipulated training ...
Early planning prevents expensive corrections when startups address clinical strategy, regulatory pathways, and cybersecurity requirements from day one rather than improvising solutions before launch. FDA pre-submission ...
Quality management system implementation delays create cascading failures across medical device development timelines. Startups using SharePoint or Google Drive for documentation discover at audit time that these tools p...
Early design decisions define the trajectory of a medical device long before commercialization begins. Choices related to software architecture, third-party components, and system connectivity establish both the opportun...
Alarm fatigue happens when monitoring systems raise so many false flags that clinical staff begin ignoring them, even when real critical events occur. A surgeon during an operation gets alarms indicating patient bleeding...
Devices that do not integrate into the clinical workflow sit unused regardless of technical sophistication. Physicians work in high-pressure environments where equipment must be 100 percent reliable, secure, and enhance ...
Marketing medical devices requires understanding that stakeholders are different, buying processes are longer, and friction points are more complex than consumer products or software. Most companies build websites and at...
Medical device risk assessments are failing patients, not because the process is too hard, but because nobody doing the assessment has ever been in the room where the device actually gets used.Medtech quality and regulat...
Ten years ago, Singapore's healthcare system got hacked. Patient records were stolen at a national scale. The government responded by building one of the most comprehensive medical device security frameworks in the world...
SBOMs are one of the most common sources of FDA deficiencies in medical device submissions. Most companies think they're doing it right, but then they get feedback asking for missing components or clarification on what's...
Building medical device software is hard. Building it the right way is harder. And getting it through FDA approval while managing cybersecurity requirements? That's what Darcy Bachert has been doing for 17 years.Darcy ru...
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