Roadmap of Research Life Cycle

This research roadmap offers all researchers in Amsterdam UMC structured information on setting up, carrying out and completing scientific research, including clinical trials. What requirements do you have to meet for each kind of research project? And what kind of support is available from Amsterdam UMC?

Search in all subjects

Information that specifically applies to WMO or Non-WMO research is marked by a colour.

WMO Research is subject to the WMO if the following criteria are met: 1. It concerns medical scientific research and 2. Participants are subject to procedures or are required to follow rules of behaviour.
Non-WMO Research that does not fall within the scope of WMO legislation. Non-WMO research includes scientific research in which e.g. research data is collected by studying medical records.

News

Mijn studie is geautoriseerd in CTIS. Wat zijn nu belangrijke vereisten?
Mijn studie is geautoriseerd in CTIS. Wat zijn nu belangrijke vereisten?
Is uw geneesmiddelenonderzoek al overgezet naar CTIS? Wacht niet te lang - doe het nu!
Is uw geneesmiddelenonderzoek al overgezet naar CTIS? Wacht niet te lang - doe het nu!
Development and launch of a new BROK® course by GCP central
Development and launch of a new BROK® course by GCP central

Harmonized study medication rates and study medication Epic
Harmonized study medication rates and study medication Epic
Dutch Trial Register (LTR) becomes Overview of Medical Research in the Netherlands (OMON)
Dutch Trial Register (LTR) becomes Overview of Medical Research in the Netherlands (OMON)
Transition trials: CTD to CTR
Transition trials: CTD to CTR

All news

  • BI dashboard Research
  • Research Manager
  • CTIS Portal
  • Doctoral School
  • CCMO (Centrale Commissie Mensgebonden Onderzoek)
  • APH quality handbook
  • ToetsingOnline
  • Epic and Research (tipsheets)
  • MREC Amsterdam UMC
  • Health RI - ELSIE servicedesk
  • The PostDoc portal
  • The PostDoc network