Testing Standards
Advanced analytical methods ensuring product quality and safety
All products undergo comprehensive testing using advanced analytical methods and international standards
All raw materials undergo rigorous testing before use in production to ensure purity and quality standards
Continuous monitoring during manufacturing to ensure consistency and adherence to specifications
Comprehensive analysis of final tablets including potency, dissolution, and physical characteristics
Long-term shelf-life verification under various temperature and humidity conditions
Sterility and contamination checks for bacterial, fungal, and other microbial presence
Detection and quantification of any impurities to ensure product safety and purity standards
| Test Method | Purpose | Standard |
|---|---|---|
| HPLC (High-Performance Liquid Chromatography) | Ensures accurate active ingredient content in every tablet | USP/BP/IP |
| Dissolution Testing | Verifies proper tablet dissolution for optimal bioavailability | USP/BP/IP |
| Hardness Testing | Measures tablet strength and durability | USP/BP/IP |
| Friability Testing | Ensures tablets don't crumble during handling and packaging | USP/BP/IP |
| Weight Variation | Confirms uniform tablet weight within acceptable limits | USP/BP/IP |
| Moisture Content | Determines water content to ensure stability | USP/BP/IP |
| Microbial Limits | Tests for bacterial and fungal contamination | USP/BP/IP |
| Related Substances | Identifies and quantifies impurities and degradation products | USP/BP/IP |
Our commitment to rigorous testing ensures every batch meets the highest international standards
Learn More About Our Testing