What are the responsibilities of the Medical Manager?
The biobank medical manager is responsible for the various responsibilities imposed by the Royal Decree…
Who is the Sponsor of a clinical trial?
A person, company, institution or organisation that takes the responsibility to start, coordinate and/or finance…
What is the difference between a single-center and multicenter trial?
Single-center trial: a trial conducted according to a single protocol and at a single site.…
Who can provide me with an insurance certificate?
HIRUZ Clinical Trial Unit provides, on request, an insurance certificate for trials of which Ghent…
For which studies does the sponsor need to be recognised as non-commercial sponsor in Belgium and how should this recognition be requested?
For academic studies under the Belgian experiment law (May 7th 2004), the Clinical Trial Regulation…
An introduction to the Clinical Trial Regulation (CTR) – 24 April 2023
An introduction to the Clinical Trial Regulation (CTR) 24 April 2023 11:30 - 13:00 Aim:…
Infosessions: Research Portal 2023
Info sessions (Dutch) will be organised at the following times: Thursday 16 March 2023 from…
Koning Boudewijn Stichting – Research on biochemical action mechanisms in cancer
In 2023, all Funds together will give two grants of maximum € 165.000 each, covering…
New ICF templates available
New ICF templates available for clinical experimentes and trials. Templates clinical studies
HIRUZ Biobank becomes UZ Gent Biobank
UZ Gent has established a new departement, the Human Body Materials. This department combines several…
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