Scantox delivers services in full compliance with the internationally recognized OECD Good Laboratory Practice (GLP) standards. For over 25 years, our Danish facility has been licensed by both the Danish Medicines Agency (DMA) and The Danish Accreditation Fund (DANAK), reflecting our long-standing commitment to quality and regulatory excellence.
In Denmark our GLP operations are routinely inspected by Danish authorities every two years, ensuring continuous adherence to the highest standards. In addition to these official inspections, we welcome regular audits from our clients’ quality assurance teams, reinforcing transparency and trust. In our Gothenburg facility inspections are done by the Swedish authorities, and at Gentronix in the UK inspections are carried out by the British authorities.
GLP certificates issued by the monitoring authorities are available upon request, providing clear documentation of our compliance and reliability.
Our GLP Services
We offer a full suite of GLP services tailored to your development needs:
- Toxicology Studies: Acute, sub-chronic, and chronic toxicity evaluations
- Pharmacokinetics & ADME: Absorption, distribution, metabolism, and excretion profiling
- Bioanalytical Services: GLP-compliant method development and validation (e.g., LC-MS/MS, ELISA, qPCR)
- Dose Formulation Analysis
- Immunogenicity Risk Assessment
- Safety Pharmacology & Biomarkers
All studies are conducted in our certified GLP facilities with robust quality assurance oversight.
Onsite Archive
At Scantox A/S, we maintain a fully GLP-compliant archive on-site, ensuring the secure storage of all study materials in accordance with regulatory requirements. Materials are retained for the duration mandated by the Danish authorities, but we also offer flexible archiving options tailored to your specific needs.
Whether you require extended retention for long-term studies or customized access protocols, our archive is designed to support transparency, traceability, and full regulatory compliance throughout the lifecycle of your research.
Quality Assurance you can trust
- Continuous compliance with GLP standards
- Rigorous documentation and audit trails
- Inspection readiness for regulatory reviews
We offer comprehensive GLP-compliant services designed to support your product development from early-stage research through regulatory submission. Good Laboratory Practice (GLP) ensures the integrity, reliability, and traceability of non-clinical safety data, and we adhere strictly to OECD, FDA, and EMA guidelines.
Our GLP studies cover a wide range of preclinical testing, including toxicology, pharmacokinetics, bioanalysis, and safety pharmacology. Whether you’re evaluating acute or chronic toxicity, assessing ADME profiles, or validating bioanalytical methods, our experienced scientists and quality assurance teams ensure every study meets the highest standards of compliance and scientific rigour.
We operate in state-of-the-art facilities equipped for complex and high-throughput studies. Our processes are designed to be efficient and transparent, with robust documentation and audit trails that support inspection readiness and regulatory confidence.
Clients across pharmaceuticals, biotech, medical devices, agrochemicals, and environmental safety sectors trust us to deliver data that is not only scientifically sound but also fully compliant with global regulatory expectations.
Let’s work together to accelerate your development timeline while ensuring your data stands up to scrutiny. Reach out to discuss how our GLP services can support your next project.
