Pharmaceutical Laboratory Services
Diasys Labs offers accurate, cost-effective, comprehensive analytical testing services and method development for all types of pharmaceutical products, backed by expert technical support. With extensive experience in pharmaceutical chemical analysis, we are a trusted partner to manufacturers, packagers, raw material suppliers, and formulators across Canada and internationally.
Our team supports nearly every stage of the drug development process—delivering accurate, reliable, and regulatory-compliant results.
Our laboratories are GMP-compliant and provide critical services such as:
Our laboratories are GMP-compliant and provide critical services such as:
- Method Validation and Development
- Stability Testing
- Raw Material & Finished Product Testing
- Impurity Profiling
- Dissolution Testing
Our testing capabilities include:
- Characterization of active pharmaceutical ingredients (APIs), excipients and drug intermediates and products
- Quantification of impurities in raw materials and active pharmaceutical ingredients (Thermogravimetric Analysis (TGA))
- Non-destructive testing (Near-infrared Spectroscopy (NIR))
- Impurity analysis and profiling
- Dissolution profiling
- Residual solvents analysis in API and drug products
- Heavy metals
- Microbiological analyses
- Microbial limits testing
- Preservative efficacy and anti-microbial effective studies
- Zone inhibition studies
- Stability indicating method development, method transfer and validation studies
- Stability protocol preparation, analysis, and monitoring
- Cleaning validation
