MedTech Leading Voice - Webinars
MedTech Leading Voice - Webinars is an archive of recorded webinars from MLV featuring leading subject matter experts in the medical device, regulatory, and technology sectors.
Breakthrough Device Designation in the EU: A New Regulatory & Market Access Pathway
Clinical Data Transferability Strategies for Leveraging Evidence
Building a MedTech Market Pathway: Aligning Regulatory, Reimbursement, and Commercial Teams Early
Navigating the eIFU Regulation 2025/1234: Strategic Implementation Across Product Portfolios
Due Diligence for Investors: Investing in MedTech for the First Time
Spotlight on Enhancing Risk Management Throughout the Product Lifecycle
FDA Strategy 2025: Policy Pressures and the Path to MedTech Clearance
EU AI Act Countdown: Critical Actions Medical Device Companies Must Take Before 2027
MDSAP Compliance Simplified – Avoiding Audit Pitfalls & Navigating Global Jurisdictions | Replay
Cybersecurity Compliance for Connected Devices – FDA, CRA, PSTI & New Engineering Burdens | MedTech
Software-Enabled Medical Devices – Development, Cybersecurity & Regulatory Strategy | Cybermed
Digitalizing MDR Compliance – Notified Bodies, AI, and the Future of Tech Docs | MLV Webinar Replay
Too Little, Too Late? What It Really Takes to Launch a MedTech Product | LeanRAQA Webinar Replay
The Many Faces of Audits – FDA QMSR, ISO 13485 & MDSAP Demystified | Michelle Lott Webinar
Post-Market Clinical Studies in Non-Traditional Settings – Strategy, Risk & Real-World Evidence
CE Certification vs FDA Strategy Webinar
Cyber Device Global Risk & Security Summit (medical device cybersecurity webinar)
The Best of 10x Medical Device Conference 2024
Mastering PRESUB: FDA Pre-Submission for the MedTech Industry with Michelle Lott, RAC (Webinar)
Definitive MDSAP Program Update: Strategies for Global Compliance & Market Success
Mastering FDA eSTAR Cybersecurity Requirements for 510(k) Submissions
QMSR Masterclass: What You Need to Know (Webinar Replay)
How to Grow Your Regulatory | Quality product or service business
Mastering Post-Market Surveillance: TOUGH QUESTIONS Super Roundtable
Hoodin 360 Surveillance and Vigilance Platform
MLV Interview with Joe Hage, Chairman of MDG (360k members) MedTech Community (Part 1 of 5)
Huma.AI - Diversity Webinar Q+A - Biological Differences Between Minority Groups in Clinical Trials
Huma.AI - Webinar - The Path to Greater Diversity in Clinical Trials