The European Medicines Agency (EMA) is encouraging the use of new approach methodologies (NAMs) as an alternative to animal testing in the assessment of safety and efficacy of new medicines during non-clinical development (1). In the European Union (plus Norway), 8.48 million uses of animals for scientific purposes occurred in 2022 (2). In most countries, the use of animals for some safety tests is required. For instance, 

 requires marketing authorisation holders to integrate the 3Rs (replacement, reduction, refinement) and welfare standards for the treatment of animals in all aspects of the development, manufacture, and testing of medicines (3). In October 2023, EMA published a concept paper on the revision of the guideline on the principles of regulatory acceptance of 3Rs testing approaches (4). Such alternative methods as NAMs can be highly effective at modelling individual aspects of safety and efficacy and should help to reduce and/or replace animal testing in line with the 3Rs principles (5). These principles include:

Availability of a defined test methodology (protocol, endpoints)

Description of the proposed NAM context of use (i.e., the circumstances in which the NAM is applied in the development and assessment of human or veterinary medicinal products)

Establishment of the relevance within that particular context of use

Demonstration of NAM reliability and robustness (5).

NAMs will need to be phased in. EMA is working with NAM developers to facilitate regulatory acceptance of these methodologies through briefing meetings and discussions with its Scientific Advice Working Party. Companies can also apply for the Committee for Medical Products for Human Use qualification of NAMs and voluntarily submit data generated from NAMs to the EMA; however, these data can be excluded from the regulatory decision-making process (

The European Federation of Pharmaceutical Industries and Associations (EFPIA) endorses EMA's actions and believes it is feasible to phase out animal testing, “providing there is cross-sector collaboration, robust funding and incentives, global harmonization and streamlined regulatory acceptance of nan-animal methods” (6). In June 2025, EFPIA published pharma-specific recommendations regarding the phasing out of animal testing for chemical safety assessment. These include:

Strengthen collaboration between industry, regulators, academia, and non-government organisations (NGOs) through targeted consortia and incentives that catalyse NAM development.

Improve data sharing by creating safe harbour mechanisms, secure databases, and fee waivers for exploring novel methods.

Update regulatory frameworks to recognise the “last resort” principle, incorporate flexible qualification pathways, and align the roadmap with ongoing legislative revisions.

Institutionalise regular guideline reviews (e.g., every three years) to continuously phase out legacy animal tests and accelerate acceptance of new methods.

Build public trust by raising awareness of cutting-edge, non-animal approaches that can yield superior, more human-relevant safety data (6).

NAMs encompass a range of techniques, such as high-throughput screening, 

 modelling, often utilizing artificial intelligence and machine learning. NAMs focus on identifying changes in biological function that occur before outward symptoms, allowing for a more mechanistic understanding of the biomolecular interactions along the pathway toward harm (7). For instance, adverse outcome pathways (AOPs) enable tiered testing at multiple biological levels, increasing the overall predictive power and providing more accurate evidence-based approaches for hazard and risk assessment (

). AOPs could potentially reduce the levels of drug attrition rates resulting from undesired effects later in product development (8–10).

Furthermore, some organoids, organ-on-a-chip (OOC) technologies, and multi-organ microphysiological systems can simulate native organ structure and function, providing a cost-effective and accurate model for pharmacokinetics, pharmacodynamics, and toxicity studies (11). OOCs allow the rapid screening of multiple drug development candidates on a single chip, improving regulatory safety assessments and reducing the number of animal-based screens (12). In addition, several 

 cell biotransformation assays (CTAs) can assess carcinogenicity and exhibit good correlation with rodent bioassays. The CTAs can detect genotoxic and non-genotoxic carcinogens and provide a quick and more cost-effective alternative to 

 carcinogen models (13). Large pharma companies, such as AstraZeneca, GSK, and Pfizer, have established partnerships with OOC and CTA companies to harness this technology in their preclinical drug development programmes (14–16).

There is a paradigm shift toward a more mechanistically driven approach to toxicity testing for safety assessment. During the past decade, significant progress has been made in the development and evaluation of AOPs, OOCs, and 

 modelling technologies that enable risk-free biomedical testing and reduce the need for animal-based models (2). Stakeholders will need to work together to phase in NAMs and phase out animal testing (6). The regulators are keen to embrace new methodologies that replace, reduce, or refine the use of animals in research and encourage NAM developers to share their data and knowledge to facilitate the regulatory acceptance of these methodologies and ensure the NAMs are scientifically sound and useful in regulatory decision-making for the future (1).

Regulatory Acceptance of New Approach Methodologies: How to Interact with EMA

Directive 2010/63/EU of the European Parliament and of the Council of 22 September 2010 on the Protection of Animals Used for Scientific Purposes Text with EEA Relevance

Concept Paper on the Revision of the Guideline on the Principles of Regulatory Acceptance of 3Rs (Replacement, Reduction, Refinement) Testing Approaches

Guideline on the Principles of Regulatory Acceptance of 3Rs (Replacement, Reduction, Refinement) Testing Approaches.

EFPIA Recommendations on Phasing Out Animal Testing for Chemical Safety Assessments.

Adverse Outcome Pathway Networks as the Basis for the Development of New Approach Methodologies: Liver Toxicity as a Case Study.

Pathways-Based Approach Across the Biosciences–Toward Application in Practice

Adverse Outcome Pathways Can Drive Non-Animal Approaches for Safety Assessment

Organoids and Organs-on-Chips: Recent Advances, Applications in Drug Development, and Regulatory Challenges

Liver-on-a-Chip: Considerations, Advances, and Beyond

Cell Transformation Assays for Prediction of Carcinogenic Potential: State of the Science and Future Research Needs.,

Medera’s Novoheart Releases Latest Cardiac Screening Innovation, CTScreen v1.5 to Advance High-Throughput, Automated Human-Based Drug Testing

GEN. Engineered Heart-on-a-Chip Replicates Drug Responses Found in Adult Humans. 8 Aug. 2019.

Scientists Mimic Human Organs on Microscopic ‘Chips’ That Enable Drug Testing

Cheryl Barton, PhD, is founder and director of PharmaVision, Pharmavision.co.uk.

Articles

The European Medicines Agency (EMA) is promoting new approach methodologies (NAMs) to reduce animal testing in drug development, aligning with the 3Rs principles of replacement, reduction, and refinement. NAMs, including high-throughput screening, in vitro assays, and in silico modeling, offer mechanistic insights into drug safety and efficacy. The European Federation of Pharmaceutical Industries and Associations (EFPIA) supports phasing out animal testing through collaboration, funding, and regulatory updates. Techniques like organ-on-a-chip and cell transformation assays are advancing, providing cost-effective, human-relevant models for pharmacokinetics and toxicity studies.

EMA is phasing out animal testing and is asking pharmaceutical companies to use new approach methodologies.

EMA Encourages Use of New Approach Methodologies to Reduce Animal Testing 

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EMA Encourages Use of New Approach Methodologies to Reduce Animal Testing