GAIA Healthcare FZ LLC’s scientific division is dedicated to providing regulatory support for a wide range of healthcare products. They have a comprehensive understanding of the Gulf Cooperation Council (GCC) Drug Regulatory Affairs (DRA) requirements, including electronic Common Technical Document (eCTD) submissions, handling minor site and product variations, and managing these processes efficiently. They also offer services related to pharmacovigilance system implementation services, assisting clients in setting up robust systems to monitor, assess, and manage the safety profile of healthcare products. Their strengths lie in their extensive experience, insights into local legislation, knowledge of GCC DRA requirements, efficient regulatory procedures, handling complex requirements, pharmacovigilance services, and expertise in securing formulary inclusion. These qualities make them a trusted partner for regulatory support, registration, product life cycle management, and maintaining approvals for a diverse range of healthcare products.