Leading the Pursuit of New Approach Methods

For over 75 years, we have championed innovation in biopharmaceutical research. Our commitment to animal welfare is grounded in the 3Rs principles—Replacement, Reduction, and Refinement—and guided by a deep sense of responsibility. Together with our clients, we’re laying the foundation for a future where more patients gain access to life-saving treatments—safely, swiftly, and with reduced, and eventually eliminated, reliance on animal use in research.

We actively invest in and advance alternatives to animal testing that minimize impact while upholding scientific rigor and patient safety. Through the creation of a global, cross-functional Scientific Advisory Board led by Dr. Namandjé N. Bumpus, we are driving responsible innovation in New Approach Methodologies (NAMs). This board brings together Charles River’s industry-leading experts in animal welfare, science, technology, operations, and regulatory affairs, to guide our strategic direction and accelerate progress in this area.

Headshot of Namandjé Bumpus The creation of our Scientific Advisory Board marks an important step in advancing New Approach Methodologies. By bringing together leading experts across disciplines, we are ensuring that Charles River remains at the forefront of responsible innovation, guiding the development and adoption of alternatives to animal testing that uphold scientific integrity and patient safety.”

Dr. Namandjé Bumpus 

In vitro models and approaches

These computational platforms enable faster, cost-effective evaluations of safety and efficacy, serving as powerful alternatives to animal testing and helping reduce reliance on in vivo methods.

Human intestinal organoids are being used as an in vitro alternative in antiviral toxicity testing
Retrogenix® Platform: A proprietary non-human protein library that helps de-risk in vivo studies and improve non-human species selection. This technology has played a crucial role in +100 IND submissions worldwide and has been accepted into the FDA’s Innovative Science and Technology Approaches for New Drugs (ISTAND) pilot program
3D in vitro cancer models have powered dozens of studies annually for more predictive cancer immunotherapy and targeted therapy screening
Backed by an ACC-supported grant and in partnership with MatTek, we're pioneering next-gen alternatives to animal-based inhalation toxicology. Through our strategic partnership with Bit.Bio we provide iPSC and patient-derived complex cultures and organoids for disease modeling and early toxicology

In silico tools

These computational platforms enable faster, cost-effective evaluations of safety and efficacy, service as viable alternatives to animal testing while enhancing translational relevance.

Logica®, an end-to-end solution that integrates AI-driven molecular design with advanced lab capabilities to accelerate preclinical programs. Logica leverages extensive in vitro, in vivo, and predictive modeling to deliver deeper candidate insights.
We’re transforming digital pathology with AI-powered tools like Deciphex’s Patholytix and Foresight platforms, accelerating toxicologic assessments, enhancing accuracy, and streamlining drug development for faster, data-driven decisions
Virtual Control Groups (VCG) revolutionize safety study design by replacing traditional controls and reducing animal use in safety assessment. Furthermore, through our partnership with AITIA, we are utilizing Digital Twins as synthetic control arms to enhance the design and efficiency of mouse experiments

We are committed to the continuous development and expansion of alternatives to animal testing in our portfolio of products and services.

Endosafe® Trillium™ Recombinant Cascade Reagent (rCR): An animal-free endotoxin testing solution that enhances sustainability without using animals.
PathogenBinder™ Methodology: A sentinel-free, PCR-based system for health monitoring that can eliminate the need for one million sentinel rodents annually.
Next-Generation Sequencing (NGS): In partnership with PathoQuest, we offer advanced detection of viral contaminants, providing an animal-free alternative.

Our mission extends beyond organizational boundaries. Through active collaboration with regulatory agencies, policymakers, academia, and industry partners, we advocate for systemic changes that accelerate the adoption of NAMs. Explore NAMs Partnerships

Strategic investments and partnerships enhance our ability to deliver on alternatives through identified and integrated externally developed technologies and business solutions across three strategic focus areas: in vitro tools and platforms, digital technologies, and biologic modalities
We continue to invest in alternative technologies and have strategic partnerships with leading innovators, including MaTTek, Cypre, AITIA, Bit.Bio, Valo, and Unilever.
Charles River has joined the EU-backed EASYGEN Consortium to transform CAR T therapy delivery. For clients, this collaboration means earlier insights and streamlined workflows for advanced therapies. Charles River will contribute its expertise through a 3D ex vivo screening platform, leveraging its patient-derived xenograft (PDX models) biobank and advanced imaging to ensure each therapy is safe and effective before reaching patients.

Collective Momentum in 3Rs and Alternative Methods

1976

Launch of Charles River Foundation

 
 
 
 

1984

Launch of industry's first specific pathogen free research models

1987

Oncomouse (Humanized Models) Portfolio

 
 
 
 

1997

Endosafe® acquisition
(in vitro alternative to rabbits)

1998

First Investment in Digital Pathology

 
 
 
 

2002

Established Global Animal Welfare and Training Group

2005

Introduction of Preconditioning Services

Partnership with the Johns Hopkins Center for Alternatives to Animal Testing (CAAT)

Introduced Excellence in Refinement Award

 
 
 
 

2009

Charles River Foundation's mission evolved into the Charles River Commitment to Humane Animal Research Through Excellence and Responsibility Program

2011

Implementation of in vitro Endocrine Disruptor assays

 
 
 
 

2014

Established Internal Quarterly 3Rs Award

2015

3Rs Non-Profit Initiated by Jim Foster

 
 
 
 

2016-2017

3R Collaborative Launched and Funded by Charles River

Implemented Caging and Husbandry Refinements at Scale in EU

European UnionReference Laboratory for Alternatives to Animal Testing (EURL ECVAM)

2019

Pathoquest NGS Partnership (testing alternative);

Distributed Bio Partnership (Ab platform alternative)

 
 
 
 

2020

Relaunched Digital Pathology Platform

BitBio (iPSC), Cypre (3D IO models) Human Cell Models Partnerships

2021

Charles River Major Partner for OECD Case-Study (No.367) – Leading the EPA to Replace Rat Inhalation Study Using In Vitro Data

Distributed Bio and Retrogenix Acquisitions (Non-animal Alternatives)

Release of New N=1 Program Guidance by FDA (Single Species Tox) in Response to Charles River Nonclinical Programs

 
 
 
 

2022-2023

AI-augmented Drug Discovery with Logica® (Valo Health Partnership)

Pluristyx iPSC Partnership

OoC Collaborations Emulate and CN Bio Introduced PathogenBinder

Implemented In Vitro Approaches for Human Skin Sensitization

Launched Endosafe® and Trillium™ (rCR for Endotoxin Testing)

2023

Board Committee for ORAU (Office of Responsible Animal Usage)

AAALAC Accreditation for Shanghai CRADLs

 
 
 
 

2025

Alternative Methods Advancement Project™ (AMAP™) Launch

Introduced 3Rs Implementation Award from 3Rs Collaborative

Pioneering a Future Beyond Animal Testing Because Every Moment Matters

The FDA's 2025 announcement to pilot reduced animal use in monoclonal antibody programs marked an acceleration of their perspective on NAMs in regulated science. Although the industry isn't yet able to fully move beyond animal models, Charles River is investing in technologies that bring that future closer, and we continue to invest in groundbreaking technologies that offer viable alternative methods to animal testing.

Frequently Asked Questions (FAQs) About New Approach Methodologies (NAMs)

  • What are new approach methodologies (NAMs)?

    New Approach Methodologies (NAMs) are tools that improve the predictability of the efficacy and/or safety of a therapeutic or chemical substance in humans and reduce and/or replace animal testing.

    At Charles River, we are committed to leading the industry in the adoption and validation of NAMs and over the past decade, we have made significant strategic progress in this area. Through strategic integration of NAMs and collaborative partnerships, we are fostering innovation that enables the creation of next-generation tools and approaches. These solutions not only elevate the quality of nonclinical programs but also support the global shift toward more ethical, sustainable, and scientifically robust research practices.

    Our implementation strategy focuses on embedding NAMs technologies and compatible testing platforms across both:

    • Therapeutic and preventive substances, encompassing all drug modalities within traditional and emerging areas of drug discovery and development
    • Chemical substances, including non-therapeutic compounds such as agrochemicals (currently tested) and cosmetics

    This includes:

    1. In vitro models, such as human cell-based assays, organoids, and organ-on-a-chip systems that replicate human tissue responses
    2. In silico techniques like computational toxicology, machine learning-based predictive modeling, and virtual screening to simulate biological interactions
    3. In chemico methods, such as direct peptide reactivity assays (DPRA) and oxidative stress response assays that assess chemical reactivity without the use of live cells or animals
  • How can contract research organizations support new approach methodologies?

    Contract research organizations (CROs) like Charles River play a pivotal role in advancing new approach methods by evaluating and validating new models, embedding them into drug development strategies, and ensuring they meet evolving regulatory expectations. We provide the scientific expertise, infrastructure, and flexible platforms needed to apply NAMs effectively—either alongside or as new alternative methods to animal testing—helping clients make confident, data-driven decisions and accelerate their development timelines.

  • Why are new approach methodologies important?

    NAMs are essential to the future of drug discovery and development. They enable more predictive, human-relevant data generation, reduce reliance on animal models, and support ethical research practices. New alternative methods also have the potential to identify toxicities earlier, improve clinical translation, and streamline the regulatory path, ultimately helping to bring safer, more effective therapies to patients faster because every moment matters.

  • What makes Charles River a leader in the industry for new approach methodologies?

    Our leadership in new approach methods is built on deep scientific expertise, a broad portfolio of non-GLP and GLP-compliant methodologies, and a commitment to innovation. We’ve developed a strong foundation of in vitro, in silico, in chemico, and human-relevant models that are actively used across the drug development lifecycle.

    What sets us apart is our ability to translate scientific innovation into practical, scalable solutions. We work closely with regulators, academia, and industry to ensure NAMs are not only scientifically sound but also aligned with evolving standards—helping shape the future of safety assessment and therapeutic development.

    To further strengthen this leadership, we have established a Scientific Advisory Board comprised of industry-leading experts in animal welfare, science, technology, operations, and regulatory affairs. This board guides our strategic direction in NAMs, ensuring that our approach remains at the forefront of responsible innovation and supports the development and adoption of alternatives to animal testing that uphold scientific integrity and patient safety.

  • What are the challenges with new approach methodologies?

    While NAMs offer significant potential, the industry is not yet able to fully replace traditional animal models. Key challenges include the need for robust scientific validation, broader regulatory acceptance, and the development of standardized methodologies. Successfully integrating new alternative methods into existing drug development workflows also requires strategic planning, cross-functional collaboration, and a clear understanding of their appropriate applications and limitations.

    Through initiatives like AMAP, Charles River is actively working to overcome these barriers—driving innovation, building confidence, and advancing the responsible adoption of new approach methods across the industry.