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Author: Koen Bogaert

This author has written 175 articles
Read more about the article UGENT BOF – Interdisciplinary Research Projects

UGENT BOF – Interdisciplinary Research Projects

  • Post published:23 December 2021
  • Post category:Funding Closed

The budgets for interdisciplinary research projects enables a consortium, consisting of two professors, to establish…

Continue ReadingUGENT BOF – Interdisciplinary Research Projects
Read more about the article FWO – EJP-CALL on Rare Diseases

FWO – EJP-CALL on Rare Diseases

  • Post published:23 December 2021
  • Post category:Funding Closed

Topic: ‘Development of new analytic tools and pathways to accelerate diagnosis and facilitate diagnostic monitoring…

Continue ReadingFWO – EJP-CALL on Rare Diseases
Read more about the article Webinar: REDCap v11.1.19 – What’s new?

Webinar: REDCap v11.1.19 – What’s new?

  • Post published:9 December 2021
  • Post category:Archive

Continue ReadingWebinar: REDCap v11.1.19 – What’s new?

What is a biospecimen?

  • Post published:9 December 2021
  • Post category:FAQ

Human biospecimens are defined as any biological material taken from a human individual for diagnostic…

Continue ReadingWhat is a biospecimen?

What is a biobank?

  • Post published:9 December 2021
  • Post category:FAQ

A biobank is a repository for human body material such as blood, tissue, urine and…

Continue ReadingWhat is a biobank?

End of trial reporting: who is responsible?

  • Post published:9 December 2021
  • Post category:FAQ

End of trial (i.e. the last visit of the last patient – LPLV) needs to…

Continue ReadingEnd of trial reporting: who is responsible?

Do I need to prepare a final report?

  • Post published:9 December 2021
  • Post category:FAQ

Within a year after the end of trial (i.e. the last visit of the last…

Continue ReadingDo I need to prepare a final report?

Who is the insurance policyholder of a trial?

  • Post published:9 December 2021
  • Post category:FAQ

The sponsor is, even without fault, liable for all inflicted damages to the participant (or…

Continue ReadingWho is the insurance policyholder of a trial?

What is the procedure for EC approval of a multicenter trial?

  • Post published:9 December 2021
  • Post category:FAQ

If your trial is conducted at various locations, approval by the EC for each participating…

Continue ReadingWhat is the procedure for EC approval of a multicenter trial?

Do responses to comments need to be submitted via HIRUZ CTU?

  • Post published:9 December 2021
  • Post category:FAQ

For any comments, additional questions or approval from the Ethics Committee, the Ethics Committee will…

Continue ReadingDo responses to comments need to be submitted via HIRUZ CTU?
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  • HIRUZ
    • About us
    • News
    • Events
    • FAQ
    • Infosessions
  • Contract Unit
  • Clinical Trial Unit
    • Focus Team
    • Templates
    • Clinical trials
    • Experiments
    • Medical devices
    • In vitro diagnostic medical devices
    • Thesis
  • Data Management
    • REDCap features
    • Your own REDCap project
    • REDCap Walk-in
    • Clinical Data Management Services
  • Innovation & Valorisation
    • Open calls for funding
    • Research funding
    • Research valorisation
    • Industrial collaborations
    • EU-funded projects
  • Research portal
  • Quality
  • Patient Participation