Activities per year
Personal profile
Job responsibilities
I advice public reseachers conductiong clinical drug trials on the design of trial documents and submission to authorities. I monitor trials before, during, and after data collection, and my work is based on the international guideline for good clinical practice (ICH-GCP). Additionally, my work area includes teaching healthcare professionals and PhD students in the GCP unit’s courses
Keywords
- Research and Examination Methods
Areas of expertise
- GCP
- Clinical Drug Trial
- Monitoring
- Investigation of Medical Device
- Audit
Activities
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Good Clinical Practice and Researcher Initiated Trials
Jørgensen, A. (Lecturer)
27 Jun 2007Activity: Presentations, memberships, employment, ownership and other activities › Lecture and oral contribution
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Monitoring of Researcher Initiated Clinical Trials
Jørgensen, A. (Lecturer)
15 May 2007Activity: Presentations, memberships, employment, ownership and other activities › Lecture and oral contribution
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Arrangør af: "De offentlige GCP-enheders årlige fælles workshop"
Jørgensen, A. (Organizer)
15 Mar 2005 → …Activity: Participating in or organising an event types › Participation in or organisation af a conference
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Arrangør af kurset: "GCP og forskerinitierede lægemiddelforsøg"
Jørgensen, A. (Organizer)
9 Sept 2002 → 1 Jan 2025Activity: Participating in or organising an event types › Participation in or organisation af a conference
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Den offentlige GCP-netværksgruppe
Jørgensen, A. (Member)
20 Aug 2001 → …Activity: Presentations, memberships, employment, ownership and other activities › Member of research network