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  1. File/document CRF

    CRF Case Report Form. A case report form collects all the data on a single study participant requested in the study protocol. Subscribe Contact

    Last modified: 2019-02-27 19.55

  2. File/document CRO

    CRO Clinical Research Organisation. Independent contract research organisation that carries out whole or parts of clinical studies on assignment from a sponsor. Subscribe Contact

    Last modified: 2019-02-27 19.56

  3. File/document Data management

    Data management Handling of data within a clinical study, for example. Subscribe Contact

    Last modified: 2019-02-27 19.58

  4. File/document DMP

    DMP Data Management Plan. A document on data handling activities, systems, data flows and responsibilities in a clinical study. Subscribe Contact

    Last modified: 2019-02-27 19.58

  5. File/document Double blind

    Double blind A study where neither the investigator nor the study participants know which therapy is given to a specific participant. Subscribe Contact

    Last modified: 2019-02-27 20.00

  6. File/document DSMB

    DSMB Data Safety Monitoring Board. An independent group of experts who monitor the safety of study participants and the effectiveness of a therapy during an ongoing clinical intervention study. Subscribe Contact

    Last modified: 2019-02-27 19.59

  7. File/document DSUR

    DSUR Development Safety Update Report. Annual safety report that summarises side effect reports. Completed by the sponsor. Subscribe Contact

    Last modified: 2019-02-27 20.00

  8. File/document ECRIN

    ECRIN Public non-profit organisation that links together scientific partners and networks across Europe to facilitate multinational clinical research. Subscribe Contact

    Last modified: 2019-02-27 20.01

  9. File/document Effect variable

    Effect variable Something that is being registered and measured within the framework of a clinical study. Subscribe Contact

    Last modified: 2019-02-27 20.02

  10. File/document End of trial notification

    End of trial notification Shall be sent to the Medical Products Agency no later than 90 days after the conclusion of a medicine study. Subscribe Contact

    Last modified: 2019-02-27 20.02

Search this site

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  1. / English / News / What is happening in the development initiative: Statistics and follow-up of clinical studies

    News

    Christian Thörn has been project manager for the development initiative Statistics and follow-up of clinical studies. In the interview below, Christian

    Last modified: 2019-02-20
  2. / English / News / Clinical trials day - did you know this about clinical trials?

    News

    May 20 is Clinical Trials Day. A day that draws attention to the importance of clinical research that leads to new and better treatments, medicines and medical devices. On 20 May 1747,

    Last modified: 2021-05-20
  3. / English / News / Few patients participate in medicine trials

    News

    The Swedish Research Council has analyzed the development of clinical trials with medicines in Sweden between 2010 and 2016 by focusing on the number of patients scheduled to participate in

    Last modified: 2020-02-20
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