Amendments to the Standards of in vitro diagnostic Medical Device Good Manufacturing Practices; (16 page(s), in Korean)
Implementing Guidelines on the Collaborative Procedure for the Accelerated Registration of World Health Organization (WHO) – Prequalified Pharmaceutical Products and Vaccines; (6 page(s), in English)
Certain Existing Chemicals; Request To Submit Unpublished Health and Safety Data Under the Toxic Substances Control Act (TSCA); (7 page(s), in English)
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