Regulatory services in Vietnam offer specialized Pharmacovigilance and Risk Management services to ensure the safety of pharmaceutical products in the market. These services include the collection and evaluation of adverse drug reactions (ADRs) and the development of risk management plans to mitigate potential hazards. In addition, audit and compliance services are provided to ensure adherence to both local and international regulatory requirements. Regular audits assess compliance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and other relevant regulations. These services help safeguard public health and enhance the quality of healthcare products in Vietnam. They play a critical role in the country’s pharmaceutical regulatory landscape.