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CHAMPIONS ONCOLOGY QUALITY

Our Commitment to Quality Across Every Study

At Champions Oncology, quality is not limited to a single platform or study type. It is the foundation of everything we do. From in vivo PDX studies to ex vivo platforms, multi-omics, and radiopharmaceutical research, our processes are designed to ensure consistency, reliability, and scientific integrity at every stage.

Quality Framework

Quality at a Glance

When you partner with Champions, you can expect the same level of rigor, transparency, and care across all programs, backed by proven operational standards and experienced teams.

AAALAC accreditation

AAALAC-accredited animal care and welfare standards

Full traceability

Full traceability from model or sample intake through data delivery

Built for transfer

Designed to support seamless study execution and transfer

Standardized workflows

Standardized workflows across in vivo, ex vivo, and translational platforms

Continuous oversight

Continuous oversight to ensure reproducibility and consistency

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Our Framework

Built on Proven Standards

Our quality framework is grounded in established industry standards and operational best practices, applied consistently across all services to ensure dependable outcomes regardless of study type. Champions Oncology maintains AAALAC accreditation, reflecting our commitment to the highest standards of animal care and ethical research practices within our in vivo programs. Quality is embedded into daily operations, ensuring it is continuously maintained rather than applied at isolated checkpoints.

 

One Standard

Quality Across All Platforms

We apply a unified quality approach across every area of our work.

In Vivo

In vivo PDX models are supported through rigorous model intake, verification, health assessment, controlled propagation, and standardized study execution aligned to defined endpoints with a strong focus on reproducibility and continuity.

Ex vivo

Ex vivo platforms follow controlled handling of patient-derived material, standardized assay workflows, and consistent experimental conditions to reduce variability. Multi-omics and data workflows incorporate structured data generation, validation processes, and integrated quality checks to ensure reliable, traceable outputs.

Radiopharmaceutical

Radiopharmaceutical studies are conducted with controlled study design, careful handling protocols, and consistency across dosing, imaging, and analysis workflows.
Across all platforms, the goal remains the same: generate reliable, reproducible data you can trust.

End-to-End Quality Control

Quality is embedded throughout the full lifecycle of every study, including intake and assessment with verification of materials and controlled documentation, standardized handling and processing across all platforms, aligned study execution with defined protocols and ongoing oversight, and structured data management with validation and full traceability from input to output alongside transparent reporting.

Ethical Research Commitment

We are committed to responsible research practices that support both scientific rigor and ethical standards, including implementation of the 3Rs principles (Replacement, Reduction, and Refinement), continuous review of study design to optimize resource use, and dedicated teams trained in animal care and ethical practices. This ensures quality is reflected not only in outcomes, but in how studies are conducted.

The Stakes

Why Quality Matters

Quality directly impacts the reliability and translatability of your data. Inconsistent models, poorly controlled workflows, or gaps in documentation can introduce variability that delays decisions and increases risk. Our approach is designed to minimize these risks by ensuring consistency across models, studies, and platforms, enabling more confident decision-making and reducing the likelihood of costly rework or delays.

Our infrastructure and operating model are designed to deliver consistent results across studies and programs through standardized workflows applied across all platforms, experienced scientific and operational teams, and scalable systems that support both individual studies and large programs. This consistency enables confidence in both short-term results and long-term research strategies.

Quality is especially critical when transferring studies. Our structured processes ensure continuity across all platforms, with particular expertise in PDX transitions, including detailed study review to preserve integrity and endpoints, controlled transfer and validation processes for in vivo models, and alignment to original study design wherever possible. Learn more about how this is executed in our PDX Transfer Process page, which outlines the step-by-step approach to transferring studies with minimal disruption.

We believe quality also means clarity, with clearly defined processes and timelines, regular updates across all study types, and open collaboration with your team to ensure visibility into progress and confidence in outcomes.

Our quality framework is structured to align with clear, repeatable workflows across all services, making it easy to scale programs, transfer studies, and maintain consistency across teams and locations. This enables seamless integration between platforms and supports long-term research continuity.

Quality is not a one-time deliverable. It is the foundation of long-term scientific partnership. Our approach is designed to support repeatable, scalable research across platforms, programs, and time.
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