The PMDA consists of 24 offices and 2 groups as follows: the Audit Office, Information Technology Promotion Group, Office of Safety I, Office of Safety II, Office of GMP/QMS Inspection, Office of General Affairs, Office of Financial Management, Office of Planning and Coordination, Office of Relief Funds, Office of Regulatory Science, Office of Review Administration, Office of Review Management, Office of Standards and Guidelines Development, Office of International Programs, Office of New Drug I, Office of New Drug II, Office of New Drug III, Office of New Drug IV, Office of New Drug V, Office of Cellular and Tissue-based Products, Office of Vaccines and Blood Products, Office of OTC/Generic Drugs, Office of Medical Devices I, Office of Medical Devices II, Office of Medical Devices III, and Office of Conformity Audit. [Fig. 2 Organization of the Pharmaceutical and Food Safety Bureau (PFSB) and the Pharmaceuticals and Medical Devices Agency (PMDA)]. The duties are indicated below
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