Sia Analysis is fully qualified in OECD’s GLP Toxicology Studies. Therefore, toxicity/biosafety data generated for chemicals/formulations, pesticides, pharmaceuticals, cosmetics, feed, and food additives; Studies and reports at the GLP Test Facility will be accepted by regulatory authorities in more than 90 countries, including 34 OECD member countries and all other relevant member countries.
GLP Certified Studies:
The following studies are carried out within the scope of the GLP certificate of conformity to ensure that various sponsors meet the licensing requirements:
- Acute Oral Toxicity
- Acute Dermal Toxicity
- Acute Inhalation Toxicity
- Sub-Acute Oral Toxicity (14 or 28 Days)
- Sub-Acute Dermal Toxicity (14 or 28 Days)
- Subchronic Oral Toxicity (90 Days)
- Subchronic Dermal Toxicity (90 Days)
- Chronic Oral Toxicity (180 Days)
- Carcinogenicity (2 years)
- Micronucleus Test (In Vitro and In Vivo)
- Chromosomal Aberration Test (in Vitro and in Vivo)
- Skin Sensitization Test
- Skin Irritation Test
- Eye Irritation Test
Successful toxicology studies require the input of skilled study directors, toxicologists, veterinarians, biologists, Academic advisors, and support staff. With a strong understanding of scientific toxicology, our team can effectively identify potential risk factors early in the drug or agrochemical licensing process. Our scientific team has the knowledge, experience, and equipment that shape the reliability of our work. As Sia Analysis, the toxicology team; We ensure that your products are carried out under GLP conditions nationally and internationally with the support of science and technology in the legal authority processes.
Chemical/Test Substance Types for Toxicity Studies:
- Industrial chemicals
- Agricultural chemicals
- Medicines (Biotherapeutics, Vaccines, Recombinant DNA products, etc.)
- Feed and Food additives
- Nanomaterials
- Medical devices
- Biomedical implants
- Veterinary drugs
Sia Analysis Laboratories; Within the scope of GLP, Kemalpaşa Campus provides services to many stakeholders in toxicology, biocidal, and biocompatibility analysis groups.
