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  1. 2024年7月22日 · The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and ...

  2. 2023年2月2日 · Partnerships and Collaboration. The Office of Global Policy and Strategy's (OGPS) China Office mission is to strengthen the safety, quality, and effectiveness of food and medical products...

  3. Generic Drug User Fee Amendments. Self-Identification of Generic Drug Facilities, Sites and Organizations. Share. Fiscal year 2018 reporting period for self-identification opens May 1st to June ...

  4. Terminated Recall. A Terminated Recall is a recall where the FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall...

  5. 2023年12月7日 · The FAERS Public Dashboard is a highly interactive web-based tool that will allow for the querying of FAERS data in a user friendly fashion. The intention of this tool is to expand access of FAERS ...

  6. 2023年12月29日 · Regulations help to ensure quality drug products. FDA monitors drug manufacturers' compliance with Current Good Manufacturing Practice (CGMP) regulations. This web page provides links to resources...

  7. 2023年4月19日 · GMO foods have been available to consumers since the early 1990s. Since then, the FDA, EPA, and USDA have worked together to ensure that crops produced through genetic engineering for sale to ...

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