Clinical Research Monitoring Visits and Common Issues Explained

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  • Опубліковано 17 жов 2018
  • Clinical Research Monitoring Visits and Common Issues Explained
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КОМЕНТАРІ • 14

  • @maryamzarei8274
    @maryamzarei8274 7 місяців тому

    Thank you Dan🎉

  • @BucurEST1989
    @BucurEST1989 Рік тому

    Thank you

  • @aprilchen8042
    @aprilchen8042 5 років тому +3

    very useful, Thanks Dan

  • @Christyle09
    @Christyle09 5 років тому +2

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

    • @dansfera
      @dansfera  5 років тому

      thanks, good luck at your new job!

  • @gadeboye2001
    @gadeboye2001 5 років тому

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

    • @dansfera
      @dansfera  5 років тому

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

    • @umairamin1229
      @umairamin1229 3 роки тому

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

  • @reyyajacob1049
    @reyyajacob1049 4 роки тому

    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 роки тому +1

      Usually yes

    • @zouhairallali6414
      @zouhairallali6414 3 роки тому +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 місяців тому

    What is the minimum for a site to be activated?

    • @dansfera
      @dansfera  8 місяців тому

      Irb approval and all docs. One week.