#elemental impurities testing

Maintain product shelf life and performance with Synergy Bioscience’s stability testing lab. Our ICH-compliant protocols, controlled environments, and robust data ensure accurate insight into formulation behavior over time. From early development to post-approval, we support stability at every phase.

Ensure sterility and product protection with Synergy Bioscience’s container closure integrity testing (CCIT). Our non-destructive, deterministic methods detect even microscopic leaks, supporting compliance with FDA, USP <1207>, and EMA requirements. Depend on reliable data that secures product quality and trust.

Safeguard product quality with high-precision elemental impurities testing at Synergy Bioscience. Our lab uses sensitive ICP-MS and validated methods to detect toxic metals in compliance with ICH Q3D and USP guidelines. Minimize risk and meet regulatory demands with scientifically sound results.

Accurate, reproducible dissolution testing from Synergy Bioscience ensures consistent drug release and bioavailability. Our lab supports QC and development phases with USP-compliant methods, customized media, and precise equipment calibration—delivering data that drives formulation success and regulatory alignment.

Synergy Bioscience’s Structural Chemistry lab delivers sharp, detailed insight into complex molecular architecture. With advanced analytical techniques and expert interpretation, we support your development pipeline with reliable structural validation and compound characterization. Pharmaceutical innovators count on us for confident, submission-ready data.