Supported by other departments including Test Article Formulation and Analysis, Toxicokinetics and Bioanalysis, Immunology, and Pathology, the General Toxicology Department is capable of performing a full range of toxicological evaluations. With the increasing diversity of small molecules and biopharmaceuticals, there is a growing demand for increasingly complex toxicology study programs and comprehensive design and consideration of trials.
The advantages of Moreidea are:
- Professional and highly responsible Study Directors
- Flexible study design tailored to personalized and customer-oriented requirements
- Timely, rapid and accurate tracking and reporting
Scope of Services
Moreidea provides comprehensive general toxicology studies, including:
- Dose-range finding toxicity studies
- Acute toxicity studies
- Subchronic toxicity studies
- Chronic toxicity studies
- Carcinogenicity studies
- Formulation safety studies
Animal Species
- Rodents (rat, mouse, hamster, guinea pig)
- Non-rodents (rabbit, dog, non-human primate, minipig, etc.)
Administration Routes
- Oral
- Dermal
- Intradermal
- Intranasal
- Inhalation
- Subcutaneous injection
- Intraperitoneal injection
- Intramuscular injection
- Intravenous injection
- Intra-articular injection
- Others
Special Ocular Administration Routes
- Conjunctival sac
- Intravitreal
- Retrobulbar injection
- Retinal injection
Muridda provides clients with safety evaluation services including general toxicology, safety pharmacology, reproductive and developmental toxicity, genetic toxicology, immunotoxicology, as well as pharmacokinetics and toxicokinetics, covering the entire process from drug discovery to IND and NDA submissions. Through cost-effective and efficient services, we help clients shorten experimental duration and reduce the cost of new drug research and development.
We have a professional team and practical experience in drug safety evaluation, capable of delivering high-quality data and rapid turnaround times to support various drug safety evaluation research. Toxicological studies are conducted in different animal species, and all procedures from dose design, experimental research to histology, pathology and clinical testing can be performed in accordance with non-GLP or GLP standards.