Raw Material Testing
Rigorous spectroscopic and chromatographic analysis of all Active Pharmaceutical Ingredients (APIs) and excipients upon receipt. We verify identity, purity, and assay before any material enters the production flow.
Uncompromising Quality Standards
At Finder Pharma, quality is not a metric—it is the foundation of our scientific endeavor. We adhere strictly to global pharmacopeial standards to ensure efficacy, safety, and purity in every formulation.
Quality Control Process
In-process Checks
Continuous monitoring during formulation and packaging. Parameters such as tablet hardness, friability, dissolution rates, and blend uniformity are tested continuously to ensure intra-batch consistency.
Final Analysis
Comprehensive end-product testing against predefined pharmacopeial monographs. This includes sterility testing for injectables, stability studies, and final assay verification prior to batch release.
State-of-the-Art Facilities
Our manufacturing infrastructure is engineered for precision and compliance. Built to stringent cleanroom specifications (ISO Class 5-8), our facilities utilize automated, closed-loop systems to minimize human intervention and eliminate cross-contamination risks.
Advanced HVAC systems with HEPA filtration for controlled environments.
Fully automated High-Performance Liquid Chromatography (HPLC) labs.
