A laboratory built on precision and accountability
Founded in 2018, ToxSafe Analytics has grown into a trusted partner for chemical developers, pharmaceutical suppliers, and cosmetics manufacturers requiring rigorous biological screening and regulatory support.
Safe classification at every stage of development
Throughout our history, our laboratory has classified and audited chemical formulations from high-volume manufacturers, ensuring zero downstream clinical incidents.
We provide chemical developers, pharmaceutical suppliers, and cosmetics groups with a secure advisory portal to help streamline product market launch paths.
Our expert board analyzes in-vitro outputs, evaluates potential exposure levels, and crafts structured submission dossiers ready for national health authorities.
Laboratory efficiency metrics
Monthly assay accuracy and timeline execution parameters compared directly to strict GLP industry validation guidelines.
Scientific competencies
In-Vitro Testing Infrastructure
Our certified cleanroom environments support acute toxicity profiling, cell membrane permeability audits, and spectrometry-based pathway sequencing.
Regulatory Documentation
Structured dossier preparation aligned with national health authority submission formats across the EU, FDA, and international regulatory bodies.
Computational Toxicology
Hazard Quotient modeling, dose-response analysis, and multi-compound reactivity benchmarking using validated computational frameworks.
Analytical Chemistry
High-resolution mass spectrometry, chromatographic separation, and elemental analysis for environmental and industrial compound characterization.
Biological Safety Evaluation
OECD-guideline cell viability assays and biocompatibility verification for medical devices, polymers, and synthetic materials.
GLP-Compliant Operations
All laboratory operations follow Good Laboratory Practice standards with full audit trails, chain-of-custody documentation, and traceable reference standards.
Our development timeline
ToxSafe Analytics was established with a core focus on in-vitro dermal and cosmetic modeling for the personal care and pharmaceutical sectors.
Secured ISO 17025 accreditation and expanded our chemical evaluation panel library to include industrial compound and biocompatibility screening.
Launched a dedicated chemical regulatory consulting desk staffed by toxicologists with direct submission experience across EU, US, and APAC jurisdictions.
Deployed our secure B2B portal enabling corporate clients to submit samples, track assay progress, and receive validated advisory documents digitally.
Partner with our laboratory
Whether you need a single screening panel or a full regulatory submission package, our team is ready to support your timeline.