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  • MREC Amsterdam UMC Newsletter | Edition 1 | May 2026
    MREC Amsterdam UMC Newsletter | Edition 1 | May 2026 In this edition: - New developments in the merger of METC NedMec+ - Key findings from the 2025 Annual Report - New Information Sheet for Research Participants (IRP) available as of 1 May 2026 - Overview of medical-scientific research in the Netherlands - Recent progress report when submitting an amendment - Meeting cancellations
  • Quality Assurance/CMC Newsletter - May 2026
    Quality Assurance/CMC Newsletter - May 2026 In this newsletter: - Support for starting your WMO-study - Research Helpdesk - CMC info lunches - Have the 'Start Trial' & 'Start Recruitment' dates been entered in CTIS? - Other points of attention - Annual tracer program Quality Assurance Clinical Research - Good Research Practice committee - Adore Clinical Trial Support (ACTS)
  • Interactive information lunches 2026
    Interactive information lunches 2026 Register to one or more info lunches organised by the Clinical Monitoring Center!

Archive

Interactive information lunches 2026
Prescribing study medication in Epic & drug-drug interaction check at both locations
Update: New digital intake procedure for contract applications LRS
CMC / NMO Afternoon Symposium
Newsletter Quality Assurance - September 2025
ICH GCP guideline E6 - Revision 3, 2025
Newsletter Quality Assurance - July 2025
Newsletter Quality Assurance Research / CMC - May 2025
Update: Study Medication in Epic
(Ont)regel het onderzoek symposium
Newsletter MREC / Quality Assurance Research / CMC
Newsletter Kwaliteitsborging December 2024
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!
Development and launch of a new BROK® course by GCP central
Harmonized study medication rates and study medication Epic
Dutch Trial Register (LTR) becomes Overview of Medical Research in the Netherlands (OMON)
Transition trials: CTD to CTR
Template Investigational In Vitro Diagnostic Medical Device Dossier (IMDD-IVD) available
New update of the NFU Quality Assurance Guideline for research involving human subjects
Event: Mini symposium 'Ins and outs of MDR research'
Modification of study data in the Dutch Trial Register (LTR)
Handling the publication of trial documentation in K2 iProva
Harmonized approach to non-WMO review Amsterdam UMC
Patient participation in research from March 1st, 2023
Tipsheet medical device trials and the Medical Device Regulation (MDR).
Q&A Clinical Trials Regulation and CTIS
Merged MREC Amsterdam UMC as of January 1st 2023
New Dutch Trial Register online
From January 31, 2023, all new clinical trials application with medicinal products will be submitted through CTIS