In Vitro Toxicology & NAM Implementation
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Support for method validation and adaptation under OECD Test Guidelines (TG 431, 439, 492, 498, ISO 10993-5, -23).
Study planning and GLP-compliant testing and documentation.
Consulting on regulatory acceptance and dossier preparation.
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OECD GLP and GIVIMP Consulting
Establishment of GLP-compliant study environments.
GIVIMP implementation and staff training.
Support with quality assurance, SOPs, and audits.
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Regulatory & Scientific Advisory
Expert advice on method transfer, study design, and acceptance in ISO, OECD, and EU regulatory frameworks.
Collaboration with validation bodies, EURL ECVAM, and international partners.
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Project Development and Proposal Support
Horizon Europe, EFSA, or MSCA proposals (NAMs, in vitro testing, AI-integrated toxicology).
Communication, dissemination, and exploitation planning and services by an experienced team.