• Home
  • Submission
    • WMO applicable
    • Non WMO research
    • Approval Board of Directors UMCG
    • Biobank
  • Topics
    • Adverse Events (SAEs, SUSARs, SADEs, etc.)
    • Recruiting and informing the potential subject.
    • Research with minors and incapacitated subjects
    • The role of the treating physician and investigator
  • Documents
  • Information & Contact
    • METc – bureau
    • Composition METc UMCG
    • METc UMCG meetings
    • METc UMCG Fee
    • More practical information
  • FAQ
  • News
    • Meeting dates 2021
    • Brexit and possible consequences for clinical research
    • Clinical Trial Regulation expected to apply from December 2021
    • New template Subject Information Sheet is mandatory from November 2020.
    • CCMO will be the competent authority for clinical investigations with medical devices
    • Modified procedure for submitting local feasibility declaration
    • What is the impact of the GDPR on the informed consent letter?
    • Conditions for (re)starting clinical research in healthcare institutions and CRUs aligned
  • English
    • Dutch
Menu
  • Home
  • Submission
    • WMO applicable
    • Non WMO research
    • Approval Board of Directors UMCG
    • Biobank
  • Topics
    • Adverse Events (SAEs, SUSARs, SADEs, etc.)
    • Recruiting and informing the potential subject.
    • Research with minors and incapacitated subjects
    • The role of the treating physician and investigator
  • Documents
  • Information & Contact
    • METc – bureau
    • Composition METc UMCG
    • METc UMCG meetings
    • METc UMCG Fee
    • More practical information
  • FAQ
  • News
    • Meeting dates 2021
    • Brexit and possible consequences for clinical research
    • Clinical Trial Regulation expected to apply from December 2021
    • New template Subject Information Sheet is mandatory from November 2020.
    • CCMO will be the competent authority for clinical investigations with medical devices
    • Modified procedure for submitting local feasibility declaration
    • What is the impact of the GDPR on the informed consent letter?
    • Conditions for (re)starting clinical research in healthcare institutions and CRUs aligned
  • English
    • Dutch
Search
Close

News

Opening hours during holiday season

22/12/2020

Meeting dates 2021

14/12/2020

Modified procedure for submitting local feasibility declaration

09/11/2020

Clinical Trial Regulation expected to apply from December 2021

14/09/2020
  • Home
  • Submission
  • Topics
  • FAQ
  • Documents
  • Information & contact
Menu
  • Home
  • Submission
  • Topics
  • FAQ
  • Documents
  • Information & contact

POWERED BY Wild Sea 2020