Excellence in Every Dose: Glin Pharma’s Quality
At Glin Pharma, quality is the foundation of everything we do. From research and development to final production, every step is meticulously designed to uphold the highest industry standards.
We implement rigorous quality control measures, ensuring compliance with internationally recognized guidelines such as KGMP (Korean Good Manufacturing Practice) and USP 797 for sterile compounding. Beyond regulatory adherence, our approach is built on continuous innovation, integrating advanced testing protocols, process validation, and precision-driven manufacturing techniques.
To maintain unwavering consistency and reliability, our expert teams across seven international R&D centers work relentlessly to enhance product safety, efficacy, and purity. Each formulation undergoes comprehensive testing and verification, guaranteeing that every dose meets our uncompromising quality benchmarks.
At Glin Pharma, quality is not just a promise—it’s our legacy.
PHARMACEUTICAL AUTOMATION
Automation:
Precision and Efficiency
At Glin Pharma, quality isn’t just a standard—it’s our promise. We adhere to globally recognized benchmarks, including USP 797 for sterile compounding and KGMP (Korean Good Manufacturing Practice), Korea’s regulatory framework ensuring rigorous quality control in pharmaceutical manufacturing. Beyond compliance, our approach encompasses continuous product testing, advanced R&D, validated processes, and ongoing personnel training. This relentless pursuit of excellence guarantees that our products consistently exceed the highest safety and efficacy standards.
ANALYTICAL TESTING
Analytical Testing at
Glin Pharma
At Glin Pharma, each sterile batch undergoes comprehensive analytical testing to ensure compliance with quality and safety standards. Stability studies play a crucial role in determining appropriate Beyond-Use Dates (BUD) and optimal storage conditions, preserving the integrity of our formulations.
Utilizing validated testing methodologies and advanced analytical techniques, we meticulously assess each formulation’s potency, sterility, and composition consistency. This process ensures that every dose meets established pharmaceutical standards, providing healthcare professionals and patients with a reliable and high-quality product.