At Park Pharmaceuticals, quality assurance and control are pillars of our manufacturing process, ensuring every product meets stringent international standards and client expectations. Our dedicated Quality Control department operates independently under the supervision of highly qualified professionals, committed to safeguarding product integrity and patient safety.
Our quality control system is a comprehensive, ongoing process that monitors every stage—from raw material testing to final batch release—following meticulously documented procedures defined in our SOPs in line with global pharmaceutical regulations.
We employ state-of-the-art instruments and advanced technologies for precise testing of raw materials, intermediates, and finished products. Raw materials undergo rigorous assessment upon receipt and are approved before entering production. Sampling and dispensing are conducted under reverse laminar airflow conditions to prevent contamination.
Intermediate and finished products undergo detailed testing according to validated quality specifications. Only batches meeting all criteria are released for packaging and sale. Our QC lab and processes are regularly validated and audited internally and externally to comply with WHO, GMP, GLP, and other regulatory standards.
Materials failing to meet specifications are quarantined and handled as per approved protocols, including secure storage or return to suppliers. High-potency and temperature-sensitive materials are stored under strict environmental conditions to preserve stability.
At Park Pharmaceuticals, quality control is deeply integrated into decision-making processes, contributing to continuous improvement and delivering products that inspire confidence in healthcare providers worldwide.