Safety Assessment of Pharmaceuticals and Medical Devices
Toxicology Studies for Pharmaceuticals
Ina Research offers complete support services for a full-range of non-clinical toxicity studies for pharmaceutical development, from the screening stage to preparation for clinical trials.
We can propose the appropriate study design, using minimal amounts of test article to best suit your developmental needs. The various tests required for entering Phase I clinical trials, including genotoxicity and safety pharmacology studies, can be completed, from initial testing to final report submission, in as little as 8 months.
Our team of experienced researchers includes certified toxicologists, pathologists and doctorate holders, and is supported by certified laboratory animal technicians.
- General Toxicity
- Genotoxicity
- Reproductive and Developmental Toxicity
- Carcinogenicity
- Safety Pharmacology
- Local Irritation
- Immunotoxicity
- Drug Dependency
- Toxicity of Pediatric Drugs
- Screening Toxicity
- PK and TK Screening Studies
Biological Safety Tests on Medical Devices
Ina Research conducts various biological safety studies on medical devices and raw materials.
- Cytotoxicity (extraction and direct contact methods)
- Sensitization
- Irritation
- Systemic toxicity
- Implantation
- Genotoxicity
- Hemocompatibility
- Effects of contact lenses on the cornea