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Advanced Nanosafety Assessment Services Using Human-Based Models and Predictive Analytics

Listing Description

We provide comprehensive, OECD Good Laboratory Practice (GLP)-certified nanosafety services to support the safe development, validation, and commercialization of nanomaterials and nano-enabled products.

Our offer integrates advanced human-relevant in vitro models, in vivo bridging systems, high-throughput multiplex analysis, and predictive in silico tools to deliver robust, regulatory-ready safety data. Tailored solutions are developed according to client-specific materials, applications, and regulatory needs.

A key component of our service is skin irritation testing compliant with ISO and OECD guidelines, enabling clients to meet regulatory requirements in sectors such as cosmetics, chemicals, and healthcare.

Our GLP certification ensures that all studies are conducted under strict quality, traceability, and reproducibility standards, making the results suitable for regulatory submissions worldwide.

 

Offer Details

Specifications and Deliverables:

Clients receive a complete, GLP-compliant nanosafety and toxicology package, including:

  • GLP-certified study reports suitable for regulatory submission

  • Skin irritation and corrosion testing (in vitro) compliant with ISO and OECD guidelines

  • Advanced human-based in vitro models (lung, skin, liver)

  • Nanotoxicity assessment, including:

    • Cytotoxicity

    • Inflammation

    • Genotoxicity

  • In vivo bridging studies (e.g., C. elegans)

  • Multiplex biomarker profiling (cytokines, chemokines, growth factors)

  • In silico predictive modeling, including:

    • QSAR / QSPR / QSTR

    • Machine learning and classification models

  • Comprehensive risk assessment report with regulatory guidance

  • Optional custom model development tailored to client needs

 

Value Proposition:

We enable companies to bring safer nano-enabled products to market faster by combining GLP-certified experimental testing with advanced predictive modeling.

Key benefits:

  • Generate regulatory-accepted data under GLP conditions

  • Ensure compliance with OECD and ISO standards

  • Reduce development risks and avoid late-stage failures

  • Access validated skin irritation testing for safety classification

  • Integrate experimental and computational approaches for efficiency

 

Input Required from Customer:

  • Detailed description of nanomaterial(s) or formulation

  • Intended use and exposure scenario (e.g., dermal, inhalation)

  • Regulatory framework of interest (e.g., REACH, cosmetics regulation)

  • Existing experimental or safety data (if available)

  • Specific endpoints required (e.g., skin irritation, genotoxicity)

Fields of Application:

  • Cosmetics and personal care (skin irritation & safety testing)

  • Nanomedicine and drug delivery

  • Chemicals and advanced materials

  • Food and feed safety

  • Environmental and occupational health

  • Regulatory toxicology

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Location and Map

Adress:

Av. Mte. José Veiga
Braga
Braga
4715-330
Portugal

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