Comply with global regulations
Pharmaceutical packaging materials and production process components testing service
Biological Testing
United States Pharmacopoeia USP87 88
Cytotoxicity
Irritation
Implantation
Systemic toxicity
YBB&Pharmacopoeia of the People's Republic of China
Cytotoxicity
Irritation
Sensitization
Pyrogen
Haemolysis
Systemic toxicity
Chemistry Testing
Extractable Study
Toxicological risk assessment
Method development and validation
Leachables Study
Stability testing
Packaging material change study
Packaging material screening study
Single-use infusion system compatibility study
Production-side testing services
Production-side testing services
Biocompatibility testing of disposable consumables
Sensitization
Haemolysis
Pyrogen
Cytotoxicity
Irritation
Implantation
Systemic toxicity
Disinfectant efficacy testing
China：2002 Disinfection Technical Specification, 2010 GMP Guidelines
USA： AOAC Series、USP 1072、PDA TR70
Europe： EN 1276 & 1040 、EN 1650、EN 13704、EN 13697
Abnormal toxicity
Pyrogen
PDE (Permitted Daily Exposure) reporting
Microbiology routine testing
Sterility Test
Microbial Limit Test
Bioburden Test
Bacterial Endotoxin
Microbial Identification
Media suitability
Microbial customization business
Irradiation/ethylene oxide/moist heat sterilization test
Chemical sterilization test for liquids
Antimicrobial test
Environmental monitoring
Other drug-related testing services
Other drug-related testing services
Elemental impurity studies
Elemental impurity scanning
Method development and validation
Batch release testing
Risk assessment
Other testing services
Residual solvent studies
Nitrosamine impurity research services
Special substance method development and validation
Structural confirmation and structural analysis of unknowns