Medica 2025
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Event details
MEDICA is the world's leading trade fair for medical technology and healthcare, bringing together over 5,000 exhibitors from 72 countries and attracting more than 80,000 visitors. Held annually in Düsseldorf, Germany, it serves as a premier platform for showcasing innovations in medical imaging, diagnostics, health IT, and more.
QbD Group, your life sciences partner across the entire product lifecycle
At MEDICA 2025, our team will showcase innovative solutions designed to help your business thrive across the healthcare and medical technology landscape. From ensuring compliance to accelerating market entry, we provide expertise at every stage of the product lifecycle:
- Regulatory Affairs & Compliance – Navigate complex global medical regulations with confidence, guided by our experienced specialists.
- Pharmacovigilance – Protect patients and maintain safety standards with robust monitoring and reporting systems.
- Market Access Strategies – Simplify your entry into European markets with tailored, actionable strategies.
- Quality Assurance Systems – Implement effective quality management systems that meet international standards and ensure operational excellence.
Connect with our team of experts
Stop by and connect with our experts! Whether it’s regulatory guidance, market access strategies, or quality systems, we’re here to help you navigate the fast-changing healthcare landscape.
Visit us at the exhibition or reach out today to see how we can accelerate your success in medical innovation.
Bernd Lafortune
IVD Clinical Strategy BD Manager
Bernd brings deep expertise in global regulatory frameworks and strategic planning for medical technologies. His experience spans regulatory submissions, market entry strategies, and compliance consulting.
Ivana Custic
Business Development Manager Medtech
Ivana is dedicated to ensuring robust quality management systems and regulatory compliance in the medtech space. With hands-on experience in audits, ISO standards, and risk management, she offers practical insights to strengthen product safety and performance.
Sorin Stircu
Business Development Manager Medtech
Sorin bridges clinical evaluation and regulatory pathways, balancing scientific evidence with compliance demands. His background includes guiding clinical assessments, post-market surveillance, and regulatory strategy for medical devices.
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Rose Zhao
Business Development Director China
Rose Zhao leads QbD Group’s China business development efforts, connecting global medtech and pharmaceutical innovators with regulatory, quality, and market strategy support. Her regional insight and strategic mindset help bridge East–West partnerships.
Get in touch
Have a question or need more information? We’re here to help! Fill out the form and our team will get back to you as soon as possible.
Let’s start the conversation!
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