The Medical and Regulatory Affairs team at Ewopharma is responsible for ensuring compliance with regulatory standards and managing the approval processes for pharmaceutical products in Central Eastern Europe. This team collaborates with medical representatives to provide scientific support and information, oversees pharmacovigilance to monitor drug safety, and develops strategies for successful market entry and product promotion in alignment with local regulations. Their role is crucial in bridging the gap between the company's pharmaceutical offerings and regulatory requirements, ensuring safe and effective products reach the market.
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