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Medlab Middle East 2025
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Event details
What we'll cover
- Simplifying regulatory complexity: learn how to navigate MDR, IVDR, and FDA requirements with ease, breaking down complex pathways into actionable steps for efficient product certification.
- Accelerating time-to-market: explore strategies to streamline clinical trial design, regulatory submissions, and post-market surveillance to bring your product to market faster without compromising quality.
- Ensuring clinical evidence excellence: understand how to design and execute clinical trials that meet EU standards and provide robust data for regulatory approval and market success.
- Tailored solutions for startups: discover scalable, customized services to meet the unique needs of startups, from medical writing to market entry strategy.
- From idea to patient: see how we support the entire product lifecycle, from initial strategy to post-market surveillance, ensuring your innovation reaches and benefits patients effectively.
Connect with our team of experts
We invite you to connect with our team during Medlab Middle East 2025. Whether you’re seeking regulatory advice, or simply want to learn more about the latest developments in the field, QbD Group is here to help.
Get in touch with Ivana and Bernd at Medlab Middle East 2025 or contact us today.
Ivana Custic
Self-driven, goal-oriented, creative, passionate and engaging Life Science professional with over 16 years of work experience in research, commercial services, project management & business development. Experienced in capacity building, establishing contacts, building and maintaining strong relationships with all levels of technical, operational and managerial professionals in CROs, pharmaceutical and medical device industry. Skilled in Marketing, Market Research, Business Planning, Budgeting and Sales.
Bernd Lafortune
Bernd Lafortune is an expert in in-vitro diagnostics (IVD), specializing in helping companies overcome regulatory and clinical challenges. With a bioscience engineering background, Bernd manages performance evaluation studies for IVD devices and supports global manufacturers with EU compliance as an Authorized Representative.
Passionate about advancing healthcare, Bernd focuses on generating clinical evidence for IVDR and WHO submissions, ensuring groundbreaking diagnostic devices reach European markets efficiently.
Or come and visit us at one of our other events
Can’t make it to this one? No problem! We’re always on the move, sharing insights and connecting with industry professionals.
Check out our upcoming events and find the perfect opportunity to meet us in person. We’d love to see you there!
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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