From raw material procurement and order processing to in-process controls and final shipment, every operational step is rigorously monitored to deliver assured product quality. Through continuous process improvement and strict adherence to international cGMP guidelines, we ensure our operations remain ahead of shifting global regulatory demands.
We monitor performance across the entire manufacturing lifecycle. Our quality teams conduct strict sampling and testing of raw materials, starting materials, and reagents before release. During production, detailed in-process quality checks, batch controls, and analytical characterizations (including impurity profiling and degradation studies) are executed to maintain strict process consistency.
Our state-of-the-art analytical and microbiology laboratories operate in full alignment with international pharmacopeial standards (such as USP, EP, and IP). Equipped with modern instruments subject to strict internal calibration routines, our QC labs perform comprehensive testing—including microbial limit testing, bacterial endotoxin testing (BET), stability studies, and high-precision chromatographic analyses.
Synergene Active Ingredients Corporate Office, H.No.8-2-293/82/J-III/304-O, Plot No.304, Road No.78, Jubilee Hills, Hyderabad 500033, Telangana, India
+91-40-23817500
sales@synergeneapi.com
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