Comprehensive Quality Management System
Our Quality unit encompasses Quality Assurance, Regulatory support, and Validation. Our FDA-registered facilities produce API, adjuvants, and intermediates that meet the relevant cGMP requirements of 21 CFR Part 210 and 211, and ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients. A dedicated Quality Assurance representative ensures that all applicable regulatory and quality standards and requirements are met throughout your project.