On Demand Webinar

From Concept to Market: Comprehensive Market Access Strategies for Medical Device Software

This webinar will guide you through the essential steps of market access, effective commercialization strategies, and all the critical factors needed for a successful MDSW product launch. Whether you’re a seasoned professional or new to the field, this session will provide you with the knowledge and tools to make your MDSW vision a reality.

Medical Devices

On Demand

60 min

Regulatory Affairs · Medical Devices

English

n a reality.

Don’t miss out on this opportunity to elevate your product’s market presence!

What you'll learn

Identify your market segments
Customer journey mapping
Market adoption drivers
Pricing and reimbursement insights

Learn from the best

Speakers

Join us as our expert speaker shares valuable insights and practical knowledge drawn from extensive industry experience.

Steven Van Hove

Senior Consultant Business & Communications

Steven Van Hove brings over 20 years of hands-on experience in the life sciences. Currently a Senior Commercialization Consultant and Business Strategist at QbD Group, Steven excels in driving commercial strategy, improving operations, and coaching teams to unlock their full potential. He holds a Master of Science in Bio-engineering and his career spans leadership roles in sales, marketing, customer care and customer experience where he consistently delivered impactful results across EMEA and global markets. A strategic thinker and adaptive communicator, Steven is passionate about leveraging technology to elevate commercial operations.

Register here

Keep watching

More webinars

On Demand Webinar

Entering the European MedTech Market: Why One Approval Doesn't Fit All

Regulatory AffairsMar 3, 2026

Building on QbD Group's Landing in Europe MedTech whitepaper, this webinar explains why EU market entry requires a fundamentally different approach than you might expect. We'll explore where home-market regulatory logic breaks down in Europe — with a specific focus on clinical evidence expectations, Notified Body interactions, and lifecycle obligations.

Watch now

On Demand Webinar

Drug-Device Combination Products and Article 117

Regulatory AffairsDec 17, 2024

Explore the regulatory complexities of Drug-Device Combination Products. Learn about Article 117 requirements, Notified Body Opinions, and more.

Watch now

On Demand Webinar

From Paper to Practice: Technical Documentation Essentials for Medical Device Software

Regulatory AffairsNov 20, 2024

Watch our webinar to gain practical insights on crafting essential technical documentation (TD) with confidence. We’ll take you step-by-step through interpreting MDR requirements, choosing the right accredited Notified Body, and navigating the qualification and classification process—all with a focus on your software’s Intended Purpose. Don’t miss this opportunity to ensure your documentation is not just compliant, but also clear and comprehensive.

Watch now

We use cookies to enhance your experience

We use essential cookies for site functionality and optional analytics cookies to improve our services. Read our Privacy Policy and Cookie Policy.