Workshop “Quality Criteria in Patient-Oriented Research as the Foundation for Knowledge Gain“
3 - 4 March 2015
Impressions from the workshop
The participants discussed how to ensure the research quality of clinical trials.
© DFG
In his speech, DFG President Peter Strohschneider also addressed the structural problems of medical research.
© DFG
Statements and discussion moderated by DFG Vice President Leena Bruckner-Tuderman
© DFG
The workshop provided opportunities for many stimulating discussions.
© DFG
The participants discussed how to ensure the research quality of clinical trials.
© DFG
At the invitation of the DFG, a workshop entitled “Quality Criteria in Patient-Oriented Research as the Foundation for Knowledge Gain” was held in Bonn on 3 - 4 March 2015. The event was jointly organised by the review boards (clinical trials peer review panel) and the DFG Senate Commission on Key Questions in Clinical Research. Around 70 participants from research organisations, research funding organisations and patient organisations took part and discussed how to ensure the research quality of clinical trials. The main focus was on the following areas:
- Scientific requirements and evaluation criteria for high-quality research on and with humans
- Structural and legal frameworks
- Incentives and obstacles for careers in patient-oriented research
- Prospects for clinical research from the perspective of research organisations
Further information
- Programme (in German only(Download)
- List of participants (in German only(Download)
- Summary (in German only(Download)
Workshop presentations (in German only)
- Einführung, Leena Bruckner-Tuderman, Freibur(Download)
- Qualitätsmerkmale Patienten-orientierter Forschung und ihre Bedeutung für Erkenntnisgewinn, Eva Hummers-Pradie(Download)
- Der rechtliche Rahmen im Spannungsfeld von Datenschutz und Wissenschaftsfreiheit in Deutschland, Michael Fehling, Hambur(Download)
- Klinische Forschung in Deutschland: Problemfelder aus Sicht der DFG, Frank Wissing, Bon(Download)
- Öffentlicher Zugang zu allen Daten klinischer Studien in Deutschland: Wunsch und Wirklichkeit. Vorstellung des WHO Registers DRKS (Deutsches Register Klinischer Studien), Susanne Jena, Freibur(Download)
- Impulsreferat zu Arbeitsgruppe I, Wissenschaftliche Voraussetzungen und Bewertungskriterien für qualitativ hochwertige Klinische Forschung, Daniel Strech, Hannove(Download)
- Impulsreferat zu Arbeitsgruppe II, Forscherkarrieren in der Patienten-orientierten Forschung: Anreize und Hindernisse, Achim Kaasch, Köl(Download)
- Impulsreferat zu Arbeitsgruppe III, Strukturelle Rahmenbedingungen für die Klinische Forschung in Deutschland, Michael Hallek, Köl(Download)
- Keynote Lecture, Förderung von Qualität in der Patienten-orientierten Forschung – ein vergleichender Blick in die USA, Petra Kaufmann, NINDS, Bethesda, US(Download)
- Reporting Guidelines – Warum brauchen wir sie und wie lassen sie sich implementieren? Erik von Elm, Lausanne, Schwei(Download)