Regulations governing licensing of public and private manufacturers, distributors, wholesalers and retailers of medical Products; (13 page(s), in English)
Draft Commission Implementing Decision not renewing the approval of etofenprox for use in biocidal products of product-types 8 and 18 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council; (4 page(s), in English)
Amendments to the Standards of in vitro diagnostic Medical Device Good Manufacturing Practices; (16 page(s), in Korean)
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