Clinical Research Monitoring Visits and Common Issues Explained

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  • Опубликовано: 17 окт 2018
  • Clinical Research Monitoring Visits and Common Issues Explained
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Комментарии • 14

  • @maryamzarei8274
    @maryamzarei8274 7 месяцев назад

    Thank you Dan🎉

  • @BucurEST1989
    @BucurEST1989 Год назад

    Thank you

  • @aprilchen8042
    @aprilchen8042 5 лет назад +3

    very useful, Thanks Dan

  • @Christyle09
    @Christyle09 5 лет назад +2

    Very helpful, Dan! Thank you. I’m taking notes.

    • @dansfera
      @dansfera  5 лет назад

      thanks, good luck at your new job!

  • @gadeboye2001
    @gadeboye2001 5 лет назад

    How do you conduct a typical " Protocol Training" is there a format given by the Sponsor

    • @dansfera
      @dansfera  5 лет назад

      Sometimes but usually is just a training however the cra sees fit and documented as per sponsor or cro sop

    • @umairamin1229
      @umairamin1229 3 года назад

      @@dansfera Can you elaborate on this, please? I'm thinking, "how do you conduct protocl training in 30 minutes?" Thanks.

  • @reyyajacob1049
    @reyyajacob1049 4 года назад

    Hi, I am a pharmacy graduate from India and have more than a year's experience as a CRC. Do I need to study an international course to work abroad in the field of clinical research?

    • @dansfera
      @dansfera  4 года назад +1

      Usually yes

    • @zouhairallali6414
      @zouhairallali6414 3 года назад +4

      there is no such international course for CR because each country has its own laws and regulations so you have to decide which country you want to work for and then take a CR course in that particular country

  • @odwarotobias706
    @odwarotobias706 8 месяцев назад

    What is the minimum for a site to be activated?

    • @dansfera
      @dansfera  8 месяцев назад

      Irb approval and all docs. One week.