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  • Implementation of the Regulation on health technology assessment
    The Regulation (EU) 2021 2282 on health technology assessment (HTAR) entered into force on 11 January 2022 and applies from 12 January 2025 This webpage aims at informing national authorities, health technology developers and stakeholders about the implementation of the Regulation All the information required by Article 30 3 of the HTAR will also be published on this website Press release
  • Introducing a New Distance Learning Course - United States Army
    Introducing a New Distance Learning Course A new training opportunity is available at the Human Intelligence Training–Joint Center of Excellence (HT–JCOE), which will be conducted on the SECRET Internet Protocol Router Network (SIPRNET) Blackboard Learning Management System Because of the coronavirus dis-ease 2019 pandemic, the Defense Intelligence Agency and the U S Army Training and
  • EU Health Technology Assessment Regulation
    Abstract On 15 December 2021, the European Parliament and the Council of the European Union (“EU”) adopted Regulation (EU) 2021 2282 on Health Technology Assessment (the “HTA Regulation” or “HTAR”) The HTAR is therefore current law in the EU and – through the concept of direct applicability – also law in each of the EU’s 27 Member States [i] However, as we discuss further
  • New EU rules for health technology assessments become effective
    The regulation also creates an EU framework for the assessment of selected high-risk medical devices to help national authorities to make more timely and informed decisions on the pricing and reimbursement of such health technologies EMA will support the implementation of the new piece of legislation in three areas It will: support timely conduct of joint clinical assessments (JCA) by the
  • Regulation on Health Technology Assessment (HTAR) - The European . . .
    HTAR was proposed by the European Commission in 2018, formally adopted in December 2021, and will apply from January 2025 Scope of the HTAR The legislation covers the clinical aspects of Health Technology Assessment (HTA) This means the relative clinical effectiveness of a new health technology, when compared with medicines or therapies already approved for the European market Under the
  • HTAR Capacity Building Programme - European Commission
    HTAR Capacity Building ProgrammeThe Health Technology Assessment Regulation (HTAR) (EU 2021 2282) called on the EU to support voluntary cooperation between Member States in areas such as the capacity building of national HTA systems The HTAR Capacity Building Programme has been created to: build long-term capacity expertise of EU HTA bodies, so they can execute the HTAR effectively enhance
  • Hospital Tengku Ampuan Rahimah Klang (HTAR)
    Joomla! - the dynamic portal engine and content management systemNOTIS PEMBERITAHUAN KEHILANGAN BUKU SIJIL CUTI SAKIT KERAJAAN DI HTAR Makluman: Untuk makluman pihak tuan\puan, Jabatan ini telah menerima lapor
  • htar - rcac. purdue. edu
    HTAR Index File As part of the process of creating an archive file on HPSS, HTAR also creates an index file, which is a directory of the files contained in the archive The Index File includes the position of member files within the archive, so that files and or directories can be randomly retrieved from the archive without having to read through it sequentially The index file is usually
  • EU Regulation on Health Technology Assessment
    The HTA Regulation lays the foundation for EU EEA cooperation on joint health technology assessments of relative clinical efficacy and safety (joint clinical assessments), as well as joint scientific consultations for health technology developers





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