2025 Annual Report
Annual Report
We are hiring a new Science Manager!
News

We are hiring a new Science Manager!

We are looking for a dynamic and enthusiastic scientist to join our Secretariat as Science Manager. This position offers a unique opportunity to work at the interface of science, policy, and regul...
January 2026 news from the Sec Gen
News

January 2026 news from the Sec Gen

Dear colleagues and friends, As we begin a new year, I would like to thank you for your continued engagement and trust in ECETOC. 2026 promises to be an exciting and dynamic year, and I am pleased...
HSSD Tool

HSSD Tool

This software was developed by a consortium of partners to facilitate the uptake of novel approaches to estimate aquatic threshold concentrations (e.g. the concentration at which 5% of the species are exposed above their EC50, HC5).
The Human Exposure Assessment Tools Database (heatDB)

The Human Exposure Assessment Tools Database (heatDB)

heatdb is a public directory of exposure data sources as well as available tools for exposure
NanoApp

NanoApp

ECETOC’s NanoApp is a tool designed to define the boundaries of sets of similar nanoforms and to generate a justification for the REACH registration.
Targeted Risk Assessment (TRA)

Targeted Risk Assessment (TRA)

The Targeted Risk Assessment (TRA) estimates exposures to workers, consumers and the environment that arise during a series of events.
Chronic fish case studies towards an IATA

Chronic fish case studies towards an IATA

Why? Hazard and safety assessments for the pelagic compartment often rely on in vivo studies using a single fish species, raising ethical concerns and uncertainty in terms of extrapolation....
Estimating the environmental release of Synthetic Polymeric Microparticles from Products

Estimating the environmental release of Synthetic Polymeric Microparticles from Products

Why? REACH restriction: SPM use restricted; emissions reporting required by May 2027. Gap: No analytical methods available to measure SPM emissions. Solution: Draft SPERC-based approac...
Case Studies on Reliability and Relevance Considerations during Validation of NAMs

Case Studies on Reliability and Relevance Considerations during Validation of NAMs

Why? Validation of NAMs is often overlooked despite its importance for regulatory use. Traditional validation methods are less suitable for NAMs, which focus on key events rather than apical...
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Press Release
10.03.2021

New ECETOC guidance says there isn’t any scientific justification for using chemical doses that cause pain or suffering in animal testing

Brussels, 10 March 2021 – In 21st century toxicology practice, there isn’t any scientific justification for selecting high doses of chemicals in animal tests which could result in lethality, pain, suffering or other forms of profound toxicity in any of the experimental subjects, according to a new Technical Report from the Centre for chemical safety assessment (ECETOC).

Prior to registering and marketing any new pharmaceutical, chemical, agricultural chemical or food ingredient products, manufacturers must by law generate data to ensure human and environmental safety. The testing requirements to ensure human safety vary by sector, product type and geographical region or country and many require repeat-dose testing in animals.

Dose level selection is the most important aspect of the specification of repeat dose toxicity studies.  It is about identifying relevant hazards, determination of a dose response, at which dose level there are no (adverse) effects and what level of exposure leads to risk for humans or the environment.

Repeat dose studies range in duration from 28-day systemic toxicity tests to 2-year carcinogenicity studies. Rats and mice are generally used for systemic toxicity testing, while assessments of reproductive and developmental toxicity are done in rats and rabbits.

The advice on dose level selection given in test guidelines and by regulatory authorities globally for most sectors often vary; the pharmaceutical sector is the closest to having a globally aligned approach through the International Council for Harmonisation (ICH).

The criteria used to set the highest dose level are even less well harmonised across the range of studies and geographies.  These range from approaches that can be interpreted to allow a proportion of deaths at the highest dose tested to those that encourage high dose level selection based on signs of evident toxicity.

The new report’s recommendations provide pragmatic approaches to selecting dose levels that allow accurate risk assessment and also the identification of relevant hazards, which can then be used for classification purposes.

The report recognises that different sectors have differing degrees of freedom to operate in dose level selection and this is reflected in the overall recommended approaches. These can be applied within the current regulatory frameworks, and also provide future options and approaches to science-based dose level selection. Dose selection should be based on best scientific practises as well as on social acceptance of the appropriate level of toxicity in animals to serve the above-mentioned purposes of testing

Olivier De Matos, ECETOC Secretary General, said: “The Task Force’s report provides guidance to achieve a good balance between chemical safety assessment requirements and animal welfare, while also supporting the appropriate design and interpretation of toxicity studies.”

 Download the report here.

-ENDS-