Forensic Toxicology Resource Library
Scientific guides to specimen collection, analytical methods, quality assurance, and interpretation. The topic collections below are hosted in our companion educational library at ForensicToxicology.net.
New method-focused guide: CBD-to-THC conversion during GC-MS sample preparation. For the broader collection, visit the ForensicToxicology.net evidence library.
THC testing foundations: QuEChERS extraction, recovery and accuracy explains what a full-text methods study can establish, why low detection limits need context, and why analytical validation is not an impairment test.
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Selected 2026 cannabinoid research: the THC potency and simulated-driving brief separates study design, primary and secondary outcomes, concentration-performance associations, and the limits of individual interpretation.
For question-led reading paths across the four connected sites, visit the Attorney Scientists research library. It organizes methods, specimens, alcohol, quality, and interpretation resources for readers preparing a scientific review.
Analytical methods determine how a laboratory separates, identifies, and measures a target compound. This collection connects the major procedures and quality checks that make a toxicology measurement interpretable.
A toxicology result is inseparable from the specimen that was tested. Blood, urine, oral fluid, hair, vitreous humor, tissue, and small-volume samples each have different collection, stability, and interpretation considerations.
Volatile analysis has its own laboratory language: sealed containers, headspace equilibration, gas chromatography, detector choice, preservative conditions, and specimen stability.
Postmortem toxicology combines analytical measurement with specimen-specific biology that can change after death. Collection site, matrix, decomposition, stability, and redistribution are central parts of the scientific context.
Drug analysis depends on a defined target list and a selective method. The word drug may describe thousands of chemically different compounds, so a result is only as broad as the analytes and methods actually included.
Reliable toxicology testing is supported by a quality system, not a single instrument reading. Validation, calibration, control samples, documentation, and review show whether an analytical process performed within expectations.
Interpreting a toxicology finding means describing what the analytical method actually established, then recognizing the biological and analytical limits that remain.