Triskelion
Triskelion is an international contract research organization dedicated to improving and safeguarding the health and well-being of humans and animals by ensuring the quality, safety, and efficacy of food, medicines, and chemical products. Part of the Certania Group, it offers innovative services in testing, inspections, and certifications related to food, health, and the environment, supporting product development and regulatory compliance with a focus on high-quality research and professional advice.
Industries
Nr. of Employees
large (251-1000)
Triskelion
Reactorweg 47-A, 3542 AD Utrecht, The Netherlands
Products
Quantitative gelatin species-determination method
A quantitative analytical method for determining species composition in gelatin and collagen-derived products to support label claims and species-origin verification.
Validated qPCR assay for ruminant DNA in processed animal meal
A qPCR assay validated in a European ring trial for detection of ruminant DNA in processed animal meal and accredited for use in regulatory testing under ISO/IEC 17025.
Quantitative gelatin species-determination method
A quantitative analytical method for determining species composition in gelatin and collagen-derived products to support label claims and species-origin verification.
Validated qPCR assay for ruminant DNA in processed animal meal
A qPCR assay validated in a European ring trial for detection of ruminant DNA in processed animal meal and accredited for use in regulatory testing under ISO/IEC 17025.
Services
Regulatory strategy, study design and dossier preparation for active substance approval and product authorisation under biocidal product regulations; monitoring, IUCLID support, risk assessment and authority interaction.
Method development, qualification/validation and GLP‑capable sample analysis for quantification of drugs, metabolites and biomarkers in biological matrices to support regulatory studies.
DNA- and protein-based testing for species identification, allergen detection and fraud investigations using qPCR and LC‑MS workflows; bespoke assay development for complex matrices.
Analytical testing, NIAS evaluation and preparation of regulatory petitions for food contact materials; ongoing compliance checks for national and international authorisation pathways.
Strategic regulatory advice and dossier preparation to obtain and maintain market access under REACH, CLP and plant protection product frameworks, including endocrine disruption assessments and regulatory monitoring.
On-call rapid response including emergency sampling, prioritized analyses and guidance to mitigate consumer safety risks and reputational impact.
Regulatory strategy, study design and dossier preparation for active substance approval and product authorisation under biocidal product regulations; monitoring, IUCLID support, risk assessment and authority interaction.
Method development, qualification/validation and GLP‑capable sample analysis for quantification of drugs, metabolites and biomarkers in biological matrices to support regulatory studies.
DNA- and protein-based testing for species identification, allergen detection and fraud investigations using qPCR and LC‑MS workflows; bespoke assay development for complex matrices.
Analytical testing, NIAS evaluation and preparation of regulatory petitions for food contact materials; ongoing compliance checks for national and international authorisation pathways.
Strategic regulatory advice and dossier preparation to obtain and maintain market access under REACH, CLP and plant protection product frameworks, including endocrine disruption assessments and regulatory monitoring.
On-call rapid response including emergency sampling, prioritized analyses and guidance to mitigate consumer safety risks and reputational impact.
Expertise Areas
- Analytical chemistry and mass spectrometry
- Food and feed authenticity testing
- Bioanalysis for drug development and GLP studies
- Chemical regulatory compliance and dossier strategy (REACH, BPR, PPP, CLP)
Key Technologies
- Ultra-performance liquid chromatography (UPLC/LC)
- LC–MS/MS (tandem mass spectrometry)
- High-resolution mass spectrometry (HR‑MS)
- LC‑MS methods for proteins and peptides
News & Updates
Risk assessment for disinfection by-products formed by halogen-containing biocides, highlighting challenges and frameworks for human and environmental risk assessments.
Guidance on assessing the equivalence of technical active substances in regulatory processes.
Discussion on upcoming regulatory changes in the CLP regulation and their impact on industry compliance.
Guidance on environmental risk assessment for antifouling products, including key factors and considerations.
Discussion on current assessment methods and challenges in evaluating endocrine disruption of non-active substances.
Guidance on demonstrating efficacy within biocidal product families.
Risk assessment for disinfection by-products formed by halogen-containing biocides, highlighting challenges and frameworks for human and environmental risk assessments.
Guidance on assessing the equivalence of technical active substances in regulatory processes.
Discussion on upcoming regulatory changes in the CLP regulation and their impact on industry compliance.
Guidance on environmental risk assessment for antifouling products, including key factors and considerations.
Discussion on current assessment methods and challenges in evaluating endocrine disruption of non-active substances.
Guidance on demonstrating efficacy within biocidal product families.