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Predictive Toxicology
(Q)SAR
Evaluation of the relationship between chemical structure and biological activity of compounds for exploratory and registration purposes.
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Evaluation of
Toxicological Studies
Validation of
in vivo, in vitro
and
in silico
toxicological assays for regulatory acceptance purposes.
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Technical-Scientific Support in Conducting Studies
On-site or remote monitoring of studies conducted at CROs / Implementation of Toxicological and Ecotoxicological Studies.
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Requirements and
Technical Opinions
Technical and scientific support for the preparation of defense to the requirements and technical opinions for the competent authorities.
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PATE
(Company Technical
Evaluation Opinion)
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.
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Impurity
Synthesis Process
Patent evaluation, pre-screening and screening of impurities generated during the manufacturing process.
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5-batches Study
Implementation, monitoring and evaluation of studies in accordance with current legislation, considering all processes and controls.
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Quality Assurance System
Implementation, Inspection and Auditing
• BLP
• ISO 17.025
• ISO 9001
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Product Registration HUB
Management of the entire process in South America and Mexico for the Agrochemical, Householding, Veterinary Products, Fertilizers, Growth Regulators, Food Additives and Biological Products and Agents’ markets.
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Market Evaluation
Efficient market analysis, based on current data that guide strategic planning and future decisions.
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