State Of Quality System

At SK-Pharma we provide full and comprehensive regulatory support, at all phases of the product’s lifecycle. Our experts’ scientific and analytical thinking is combined with a comprehensive range of regulatory affairs.

Regulatory Affairs Quality and Pharmacovigilance Department

K.S.Kim International Ltd. is committed to provide the market with high quality generic medicinal products, needed by so many patients. To ensure this target is met, K.S.Kim International Ltd. has formed a highly professional Regulatory Affairs Department, comprised of experienced pharmacists who put in a constantly work towards registering, releasing, and providing the market with high-standard and essential medicinal products, whilst working within the guidance of many international professional regulatory bodies. In addition, K.S.Kim International Ltd. has formed a Quality Assurance and Pharmacovigilance Department that use robust procedures and systems to ensure the company’s commitment to high standards of safety and quality is always met. As a credit to our team’s repeated proven high standards and quality of work and products, K.S.Kim International was granted a 5-year valid GMP certification in 2018.(issued by the respected Israeli Ministry of Health GMP Inspection Unit.)

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