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CellCarta Establishes Strategic Partnership with Waters to Advance Companion Diagnostics Development

Key Takeaway: CellCarta has formed a strategic partnership with Waters Corporation to enhance the development of companion diagnostics and flow cytometry programs. This collaboration aims to streamline the process from biomarker strategy through clinical development and commercialization. The partnership is particularly focused on integrating capabilities to support multinational clinical trials, especially in China.

Market Sentiment Analysis

POSITIVE FACTORS

  • Strategic partnership enhances capabilities in companion diagnostics.
  • Combines expertise of CellCarta and Waters for better clinical outcomes.
  • Focus on standardized flow cytometry can improve global scalability.

Full Press Release Details

Collaboration combines CellCarta's global clinical trial testing capabilities with Waters' standardized flow cytometry platforms and expertise
MONTREAL, Oct. 5, 2026 /PRNewswire/ -- CellCarta, a leading global CRO laboratory to the biopharmaceutical industry, today announced a strategic partnership with Waters Corporation, a global leader in life sciences and diagnostics, creating a framework to jointly pursue companion diagnostic (CDx) and next-generation flow cytometry opportunities with pharmaceutical and biotechnology companies.
The collaboration will initially emphasize flow cytometry-based programs. For CDx opportunities, the partnership aims to provide sponsors with a coordinated path from biomarker strategy through clinical development, regulatory submission and global commercialization.
The collaboration will initially emphasize flow cytometry-based programs. For CDx opportunities, the partnership aims to provide sponsors with a coordinated path from biomarker strategy through clinical development, regulatory submission and global commercialization.
The complementary expertise of CellCarta and Waters spans assay innovation, development, validation, and global implementation. Waters provides underlying technology capabilities, including instrumentation, reagents, standardized panels, assay development, software analysis, and, where appropriate, custom reagent and IVD commercialization. CellCarta leverages its extensive biomarker, translational research, and clinical development expertise to integrate and deploy the assay across its global CDx Lab Network, supporting Phase I-III clinical trial testing, generation of analytical and clinical evidence, regulatory and logistics support, and commercial laboratory services. Together, the companies aim to deliver standardized and globally scalable solutions for precision medicine.
The existing platform alignment between CellCarta's CAP-accredited laboratory's capabilities in Jining, China and BD flow cytometry platforms create a practical foundation for global sponsors seeking to include China in future multinational CDx and biomarker programs, as well as China-based biopharmaceutical companies preparing to expand their therapies and diagnostic strategies globally.
"For our biopharmaceutical sponsors, the business value of this partnership is clear: a more connected path from biomarker strategy through global clinical development and, where appropriate, commercialization," said Todd Chermak, President of CellCarta. "By combining CellCarta's end-to-end laboratory capabilities with Waters' diagnostic and CDx development expertise, and flow cytometry platforms, we can help sponsors reduce complexity, preserve program continuity and make earlier, more informed decisions about how to scale their programs. We are already engaging pharmaceutical and biotechnology companies on near-term opportunities where this combined model can make a meaningful difference."
"In particular for China, this partnership has the potential to help sponsors pursue more consistent China-to-global and global-to-China pathways while accounting for cross-border, regulatory, and operational requirements," said Christopher Ung, Chief Scientific Business Officer and Head of China Strategy for CellCarta. "Together, we can connect patient selection with treatment-response assessment—and make China part of that strategy from the beginning."
"Next-generation flow cytometry is expanding what laboratories can see by combining highly sensitive rare-cell analysis with greater standardization across the entire workflow," said Brent Gaylord, VP/GM Reagents, Waters Biosciences, Waters Corporation. "By combining CellCarta's contract research organization expertise with Waters' clinical assay development expertise and integrated instruments, reagents, and informatics, this collaboration is designed to help biopharmaceutical sponsors translate high-value cellular insights into clinical assays that can be consistently deployed across programs and geographies."

About CellCarta

CellCarta is a leading global CRO laboratory to the biopharmaceutical industry. With CAP accreditations and CLIA certifications for specific testing methods and facilities in Canada, the United States, Belgium, Australia and China, CellCarta provides a wide range of biomarker testing services and customized solutions to world-renowned pharmaceutical companies. By integrating analytical platforms in immunology, histopathology, proteomics and genomics, along with sample management and logistics services, CellCarta supports the entire drug-development cycle from discovery to late-stage clinical trials. Visit cellcarta.com and connect with CellCarta on LinkedIn and X.

Frequently Asked Questions

What is the focus of the CellCarta and Waters partnership?

The partnership focuses on advancing companion diagnostics and flow cytometry programs.

How will this collaboration benefit biopharmaceutical companies?

It offers a coordinated path from biomarker strategy through clinical development and commercialization.

What specific capabilities does CellCarta bring to the partnership?

CellCarta provides extensive expertise in biomarker research and clinical development.

How does this partnership impact clinical trials in China?

It aims to create consistent pathways for global and China-based clinical trials.

Last updated: Oct 5, 2026