Draft Commission Implementing Decision not approving 5-chloro-2-methyl-2H-isothiazol-3- one (CIT) as an active substance for use in biocidal products of product-type 6 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; (4 page(s), in English)

National Standard of the P.R.C., Sterilization of health care products—Radiation—Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices.; (23 page(s), in Chinese)

Guidelines on the Publishing of Package Insert and Patient Information Leaflet of Registered Drug Products in the Food and Drug Administration (FDA) Verification Portal System; (3 page(s), in English)