Navigating EU MDR compliance can be a frustrating and complex process for MedTech companies. In this insightful interview, top MedTech consultant Karandeep Singh Badwal shares his expertise on the latest industry trends, regulatory hurdles, and the key differences between FDA and EU MDR.

🤔 What You’ll Learn in This Video:
- The biggest challenges in EU MDR compliance
- How notified bodies impact regulatory timelines
- FDA vs. EU MDR – Which is better for innovation?
- AI and software’s growing role in MedTech
- Expert compliance tips for medical device companies

Whether you're a MedTech entrepreneur, regulatory professional, or healthcare innovator, this video provides must-know insights to stay ahead in the industry.

🔔 Subscribe now for more expert interviews and regulatory updates!

📌 Useful Links:
EU MDR
US FDA: De Novo Classification
US FDA: Premarket Notification 510(k)
RSNA – Radiology Event
LinkedIn Creator Accelerator Program

⏱️ Timestamps:
(0:00) Intro
(2:30) From Royal Air Force to MedTech: A Unique Career Shift
(7:45) Lessons on Delayed Gratification in Business
(12:15) EU MDR Compliance & Challenges
(16:30) The Realities of MedTech Consulting
(22:00) AI & Software’s Role in the Future of Medical Devices
(27:00) Final Thoughts: Building a Legacy in MedTech

📢 Follow the Experts on LinkedIn:
Harsh Thakkar
Karandeep Singh Badwal 

For transcripts, check out the podcast website - www.lifesciencespod.com