Our lab capabilities are second
to none.

"We treat your product as if it were our own."

Simone Blair, Senior Manager
Business Development Canadian Operations

 

 

 

 

Method Development and Validation

Our highly skilled team can examine and troubleshoot challenging analytical requirements. We can execute a client specific protocol or follow our internal Standard Operating Procedure. Methods are validated in compliance with current ICH guidelines.

• Method Development
• Method Validation
• Cleaning Validation
• Method Transfer
• Forced Degradation Studies

Analytical Testing

We offer a comprehensive range of analytical services for routine product release and stability studies.

• HPLC
• GC
• Ion chromatography
• Dissolution
• UV spectrophotometry
• FTIR spectrophotometry
• TLC
• Wet chemistry

Microbiological

Our skilled microbiology staff can meet the needs of routine pharmaceutical requirements.

• Microbial limit testing
• Antimicrobial Effectiveness Testing (AET)
• Preparatory testing

Stability Studies

Innopharm can design and manage comprehensive stability studies that follow the ICH guidelines. Conditions offered include:

• 25°C ± 2°C / 60% ± 5% relative humidity
• 30°C ± 2°C / 60% ± 5% relative humidity
• 30°C ± 2°C / 65% ± 5% relative humidity
• 40°C ± 2°C / 75% ± 5% relative humidity
• 30°C ± 2°C ambient
• 40°C ± 2°C ambient
• 50°C ± 2°C ambient