Greenlight Guru

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Greenlight Guru is the #1 provider of modern cloud-based solutions for the MedTech industry, helping companies bring life-changing products to market faster,...

Latest Videos

Switching Careers to MedTech A Practical Guide for Engineers and Professionals

Building a MedTech Powerhouse The 5 Stages of Founder Success

Human Factors vs. Clinical Trials Why Your MedTech Submission is Stalling

7 Pitfalls of International MedTech Expansion

MedTech Investment Outcomes, Regulations, and the Shift to At-Home Care

Solving the Pediatric MedTech Gap with Edwin Lindsay

The Hidden Physics of the MedTech Life Cycle with Dr. Kristy Katzenmeyer-Pleuss

ISO 10993-12025 What Risk-Based Biocompatibility Means for MedTech

Generative AI in MedTech Quality, Risks, and the Autonomy Scale with Ashkon Rasooli

Scaling Your QMS What the FDA Really Expects for MedTech Startups

MedTech Leadership Vulnerability & The CEC Framework with Dr. Jenny Hoffmann

The Role of AI in Clinical Operations for MedTech

After QMSR what FDA investigators will look for, and how to prepare your post-market team now

MedTech AI Trends 2025 Scaling Regulatory Intelligence with Michelle Wu

Balancing Innovation and Compliance in Medical Device Development

Right data in, right decisions out mastering chemical characterization for safe medical devices

Navigating AI in medical devices & healthcare – from hype to harmonization!

Countdown to QMSR What you need to know to be ready for February 2026

What's So Special About The “Special” 510(k) Why are fewer s510(k)’s being submitted today

Software as a Medical Device Building for Compliance and Innovation

Inside the investor’s mind What VCs look for in medtech and life sciences startups

Compassion and compliance in the conduct of clinical research

Clinical Submission Do's & Don’ts Tips from a Former Notified Body Expert

Live with FDA Accelerating a Quality Culture at Your Medical Device Company

Significant Risk vs. Nonsignificant Risk Devices What’s the Difference & Why Does It Matter

How to make the right clinical trade-offs between FDA and EU MDR

Managing multiple partners in product development strategies for success

CAPA vs. PACA Which is the smarter approach

Key regulatory insights for US and EU market access

Manufacturing of medical devices, design transfer and heading into the unknown