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Free Sepsis Diagnostics Webinar – The Future of Rapid Pathogen Identification

Illustration showing bacteria circulating inside a blood vessel, representing bloodstream infection and sepsis.

Are you working with sepsis, bloodstream infections, or molecular diagnostics? Join us on Tuesday, May 20 at 10:00 AM (GMT+2) for a free, expert-led sepsis diagnostics webinar focused on the promise and pitfalls of rapid pathogen identification.

Despite advances in molecular diagnostics, conventional blood culture remains the standard in clinical microbiology — even with its known limitations in speed and sensitivity. This webinar explores what’s next.


🧬 What You’ll Learn

  • ✅ Why conventional methods still dominate clinical practice
  • ✅ What molecular diagnostics offer — and where they fall short
  • ✅ Emerging tools for faster, more accurate sepsis detection
  • ✅ Real-world insights from clinical and commercial experts

👥 Meet the Speakers

  • Dr. Jan Gorm Lisby
    Section Chief, Department of Clinical Microbiology
    Hvidovre Hospital, University of Copenhagen
  • Dr. Flavia Huygens
    Executive Director & CSO
    Microbio (Australia)
  • Katie Shepherd
    Medical Science Liaison
    Microbio

🌍 Who Should Attend?

This webinar on sepsis diagnostics is ideal for:

  • Clinical microbiologists
  • Infectious disease researchers
  • Anyone working in sepsis detection, infection control, or molecular diagnostics

📅 Event Details

  • Date: Tuesday, May 20
  • Time: 10:00–11:00 AM (GMT+2)
  • Format: Online (Microsoft Teams)
  • Cost: Free to attend

📩 Sign Up Now

Don’t miss this opportunity to learn about the future of rapid molecular diagnostics in systemic infections like sepsis.

👉 Register here for the webinar


🔬 Why It Matters

Sepsis remains a leading cause of mortality worldwide, and faster pathogen identification can save lives. This sepsis diagnostics webinar brings together clinical expertise and new technologies aiming to revolutionize how we respond to bloodstream infections.

Ready to learn more?

Contact You Do Bio today to discuss GMP or RUO rHSA for your project needs.

Frequently Asked Questions

What makes Canvax’s rHSA “true GMP”?

It’s manufactured in Europe under full GMP compliance — not just “GMP-like.” The process includes full validation, batch traceability, and regulatory documentation.

Yes! Canvax’s RUO and GMP rHSA share consistent quality profiles, allowing a smooth, low-risk transition to GMP-grade for scale-up.

Yes, it’s a recombinant human serum albumin — animal-free and xeno-free, ideal for regulated and ethical workflows.

With over 20 years experience in the field of laboratory technology, my job is to help you reach your research goals.

You Do Bio has a diverse portfolio of products, from several companies, backed up by the inventive minds that developed them. Whatever your problem, I will work together with my suppliers to find a solution.

Author picture

Peter Roberts,

founder of You Do Bio

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