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Predictive Toxicology
(Q)SAR
Evaluation of the relationship between chemical
structure and biological activity of compounds for
regulatory and exploratory purposes.
Risk assessment:
Human Health and
Environmental
• Hazard identification;
• Dose-effect and dose-response
assessment;
• Exposure assessment;
• Risk characterization.
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Evaluation of
(Eco)Toxicological
Studies
Validation of in vivo, in vitro and in
silico toxicological assays for
regulatory acceptance purposes.
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Evaluation of Phys-Chem
/ 5-batches Studies
Implementation, monitoring and
evaluation of studies in accordance
with current legislation, considering
all processes and controls.
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FLORA - Anvisa
Optimized Reading Form in
the Pesticides Registration,
aiming to speed up the dossie
evaluation at ANVISA.
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PATE
(Company Technical
Evaluation Advice)
Assistance in the preparation of the
necessary documentation to comply
with RDC No. 184 of 10/17/2017 and
Guide No. 13/2017 - version 1 of
ANVISA. (NTP and ETP).
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Impurity
Synthesis Process
Pre-sorting and sorting of
impurities generated during the
manufacturing process.
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Requirements and
Technical Advice
Technical and scientific support for
the preparation of defense to the
requirements and technical opinions
for the competent authorities.
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Trainings and Lectures
in company
Customized trainning
towards companies needs.
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