Regulatory Affairs
About
The Regulatory Affairs team at SK Pharma ensures compliance with all regulatory requirements for the commercialization of pharmaceuticals. They handle the preparation, submission, and management of regulatory documents, including over 50 ANDA submissions annually, to gain approval from health authorities across multiple geographies such as Israel, PA, CIS, EMEA, LATAM, Canada, and the USA. This team also manages the lifecycle of pharmaceutical products, ensuring they meet the necessary guidelines and standards throughout their market availability.