2025 Rapid Diagnostic Test Development Conference

April 01-02, 2025, Vancouver, Canada

“Innovation meets Inspiration”

Mark your calendars for the Merck Rapid Diagnostic Test Development Conference, where innovation meets inspiration! Join a vibrant community of experts for a two-day deep dive into the exciting realm of rapid diagnostic tests. You’ll soak up invaluable insights on immunoassay manufacturing and get the inside scoop on everything from advanced instrumentation to the cutting-edge use of recombinant antibodies.

Curious about the latest in magnetic bead separation or how to navigate those tricky European regulations? We’ve got you covered! Our lineup of discussions will also tackle essential topics like in-process validation for biomanufacturing and microsphere selection for both LFA and CLIA applications. This isn’t just a conference; it’s your chance to connect with like-minded professionals, exchange ideas, and unlock new possibilities in the fast-paced world of point-of-care diagnostics. Have a specific question or want some troubleshooting advice? Book a timeslot for a confidential discussion with one of our assay development experts. Don’t miss out on this incredible opportunity to learn and grow—join us and be part of the action!

Here’s what’s in it for you:

• Accelerate your assay's time to market while connecting with a vibrant community of experts who share your passion for advancing point-of-care diagnostics.
• Increase your assay’s performance with cutting-edge technologies like nitrocellulose membranes, high-sensitivity detection beads and recombinant antibodies.
• Gain exclusive insights from industry leaders on the latest trends in immunoassay manufacturing and rapid diagnostic tests, and how to navigate complex regulations.
• Consult with our experts 1:1 for personalized insights.

Topics covered include:

• Instrumentation
• Risk mitigation: what to consider when choosing a supplier
• Using recombinant antibodies
• Implementing magnetic bead separation into your workflows
• Crossover of molecular diagnostics into the lateral flow assay space
• European regulations for in vitro Diagnostics
• In-process validation with LFAs for Biomanufacturing
• Sample prep and processing for immunoassays
• Microsphere selection for LFA and CLIA Applications
• Rapid Point of Care Market Overview
• Outsourcing assay development and manufacturing

Who Should Attend:

• Research, Development, and Production Scientists
• Process Engineers
• QC/QA Managers
• Diagnostic Test Manufacturers
• Tech Transfer Managers
• Production Managers

Why: Because the development of a new in vitro diagnostic is never easy.

Registration fees and payment:

EARLY BIRD: 2-day conference attendance $195 USD; lunch included (Until the 28th of February, 2025)!!!

From the 1st of March, price for the 2-day conference will be $295 USD; lunch included.

The fee will be invoiced upon registration.

Hotel Reservations:

More information on how to reserve a room at the Pinnacle Harbourfront Hotel at the group rate will be sent with your registration confirmation email.

Agenda:*

Download agenda here

* Agenda is subject to change.