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 prime target, K.S.Kim International Ltd. has formed a highly professional Regulatory Affairs Department, comprised of experienced pharmacists who put in a great deal of efforts to fulfil the company’s top goals – to register, release, and provide the market with high-standard and extremely-needed medicinal products, using compliant procedures and well-established professional communication with the competent health authorities.In addition, K.S.Kim International Ltd. has formed a Quality Assurance and Pharmacovigilance Departments that use robust procedures and systems to ensure the company’s commitment to very high standards of safety and quality.Thanks to its well proven quality management system, K.S.Kim International has been granted a five-year valid GMP certification in 2018, issued by the respected Israeli Ministry of Health GMP Inspection Unit.