Muridda’s Analytical and Bioanalytical Department boasts a highly skilled and experienced analytical team, capable of developing, validating and applying a wide range of analytical methods to provide clients with comprehensive, high‑quality testing and analytical services. As a critical platform, the Analytical and Bioanalytical Department plays an essential role in supporting the systematic development of pharmaceuticals.
Recognizing the pivotal position of analysis and bioanalysis in drug development, Muridda consistently delivers accurate, reliable and real‑time data in compliance with regulatory guidelines worldwide, ensuring the smooth progress of clients’ drug discovery, preclinical studies and clinical trials.
Test Items
- Preclinical and clinical sample analysis (GLP)
- Small molecule / macromolecule bioanalysis
- Gene analysis
- Development and validation of analytical methods for in vivo engraftment, differentiation, distribution, immune analysis and immunochemical analysis of cell therapy products
- Non‑GLP analysis
- Pharmacokinetic and toxicokinetic analysis
Analytical Platforms
- HPLC
- LC‑MS/MS
- Online‑SPE‑MS/MS
- ELISA
- ELISPOT
- EIA
- RT‑PCR
- Radiolabeling
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.