Chemical and product safety
We aim to ensure the safety
of substances and products
by increasingly using new
approach methodologies
to avoid animal testing
Innovative
chemical safety
assessments
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Regulatory
We support our clients in marketing
regulatory compliant substances
and products under the EU
Chemicals, Biocidal and
Cosmetic Product Regulations
Regulatory
compliance in
the European
Union
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We use a range of public and
commercial computational
modelling tools to predict
the physico-chemical, toxicokinetic,
and hazardous properties
of substances
QSAR modelling,
analogue
identification
and read-across
justification
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We have substantial experience
in evaluating and assessing
the endocrine disrupting properties
of substances in humans
and the environment
Evaluation
of chemical
substances
for endocrine
disrupting
properties
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Toxminds team
Our team of certified (eco)toxicology
consultants and highly motivated
research analysts closely follow the
developments in science and
regulatory toxicology to provide
state-of-the-art product safety and
regulatory compliance services
Ensuring safety
is our priority!
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Industry sectors we support

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ToxMinds News & Insights

Assessing cosmetic ingredients for endocrine disrupting properties

In the EU Cosmetics Regulation, there are no specific provisions addressing endocrine disruptors (ED) but a fitness check conducted by the European Commission (COM(2018)739) concluded that the tools foreseen in the Regulation are suitable to deal with potential health hazards connected with ED. In 2014, the EU Scientific Committee on Consumer Safety (SCCS) adopted a [...]

EFSA/ECHA (2018) guidance for the identification of endocrine disruptors (ED): looking back after the first 3 years of implementation

Guidance for the assessment of endocrine disrupting (ED) properties under the Biocidal Products and Plant Protection Product Regulations (BPR and PPPR) was published in 2018 by the European Food Safety Authorities (EFSA) and the European Chemicals Agency (ECHA)1. Adaptations of the European Chemicals and Classification & Labelling Regulations (REACH2 and CLP3) are planned, in line [...]

The importance of having a solid PC data package to support human health/environmental risk assessment and read across under REACH

Developing a solid and consistent data package for physico-chemical (PC) properties, especially when dealing with substances linked together by read across, is a crucial but sometimes underestimated part of every REACH1 registration. PC parameters are critical endpoints used for hazard, exposure and risk assessment. They are also a cornerstone of the read across approaches applied [...]

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product safety and compliance.

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