Analytical Testing
Vitane Pharmaceuticals operates an in-house Quality Control laboratory equipped to perform essential analytical tests that verify the identity, strength, purity, and physical characteristics of both raw materials and finished products. Our testing ensures that every ingredient and every batch meets required specifications before release.Our QC and technical teams work closely with clients to establish the appropriate testing protocols that support product quality, regulatory compliance, and long-term stability.
Ingredient Identification
Verification testing to confirm the identity of incoming raw materials before use in manufacturing.
Purity Testing
Screens for microbial contamination, heavy metals, and other impurities to ensure product safety.
Physical Property Analysis
Testing includes:
- Moisture content / Loss on Drying (LOD)
- Particle size distribution
- Density testing (bulk and tapped)
- Melting point (for applicable materials)
- Hardness and friability (tablets)
- Weight variation / fill weight verfication
- Disintegration time (tablets/capsules)
- pH, viscosity, and specific gravity (liquids)
Testing Capabilities & Instruments
Vitane’s in-house instruments support a wide range of analytical methods, including:
- Hardness Tester (for tablets)
- Friability Apparatus
- Disintegration Equipment
- What Analytical Testing Ensures for Your Product
What Analytical Testing Ensures for Your Product
- Confirmed ingredient identity
- Verified potency and label claim accuracy
- Absence of harmful contaminants
- Consistent physical characteristics
- Reliable manufacturing performance
- Long-term stability assurance
Vitane Performs the Following Tests:
- Raw Material Release Testing
- In-Process Testing
- Finished Product Testing
- Packaging Compatibility Checks
- Method Development (where applicable)
