Good Clinical Practice and ICH GCP Guidelines

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  • Опубликовано: 17 янв 2025

Комментарии • 12

  • @PO-cx2ej
    @PO-cx2ej Год назад +21

    For anyone who is curious, the 13 principles of the ICH GCP are the following:
    Ethics
     Trial risk vs trial benefit
     Trial participants
     Information on the Medicinal Product
     Good quality trials
     Compliance with the study protocol
     Medical decisions
     Trial staff
     Informed consent
     Clinical trial data
     Confidentiality
     Good Manufacturing Practice
     Quality assurance

  • @Omolabakegill7151
    @Omolabakegill7151 3 года назад +3

    Thank you. Well delivered

  • @TessaAvonlea
    @TessaAvonlea 3 года назад +3

    Thank you, this is really helpful

  • @raunakmukherjee5468
    @raunakmukherjee5468 2 года назад +1

    Does GCP applies to clinical feild in animal testing phase?

    • @elfreak0na1eash
      @elfreak0na1eash 2 года назад +2

      That would be covered under GLP (Good Lab Practice).
      Handling and care of test specimens (from algae to animals) is treated incredibly seriously and as with GCP, you shouldn't be allowed anywhere near the lab until you've been trained and proven your competency.

  • @mohammadyounis9615
    @mohammadyounis9615 3 года назад +1

    Do you have online courses for gcp that gives an international certificate..

    • @GCPMindset
      @GCPMindset  3 года назад +2

      Hi Mohammad. Yes we do, please have a look at our online training platform clintrain.com/ where we have listed all the different types of training including ICH GCP, specialised training for research staff. In case of any questions or something is not clear, please feel free to write us on bd@gcp-service.com. Thank you

  • @joselyn899
    @joselyn899 2 года назад +11

    She looks like lupita nyongo

  • @minigashailaja3974
    @minigashailaja3974 Год назад +2

    Hi mam iam shailaja I completed my m pharmacy and I completed training on pv and CDm j need job opportunity plz help me mam

  • @DikshaSharma-qb4es
    @DikshaSharma-qb4es 3 года назад

    Mam how we camlare inform consent form requirements ; compare ICH guidelines with germany

  • @LilsBen-f2w
    @LilsBen-f2w Год назад

    She surely does