Publications by authors named "Hartmut Krafft"

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[Main characteristics of the new authorisation procedure for clinical trials with medicinal products according to regulation (EU) no 536/2014 and the cooperation between the member states].
Thomas Sudhop, Claudia Riedel, Hartmut Krafft

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz· January 2023

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[How do stakeholders view the EU Clinical Trials Regulation one year after its implementation?].
Thomas Sudhop, Hartmut Krafft

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz· January 2023

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Clinical Development and Commercialization of Advanced Therapy Medicinal Products in the European Union: How Are the Product Pipeline and Regulatory Framework Evolving?
Tomáš Boráň, Margarida Menezes-Ferreira, Ilona Reischl, Patrick Celis, Nicolas Ferry, Hartmut Krafft

Hum Gene Ther Clin Dev· September 2017

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[The EU Portal: Implementation, importance, and features].
Harald von Aschen, Hartmut Krafft

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz· August 2017

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[Clinical Trials with Medicinal Products : Changes imposed by the new Clinical Trial Regulation].
Thomas Sudhop, Hartmut Krafft

Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz· August 2017

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Experience and further development with the Voluntary Harmonization Procedure for multinational clinical trials in the European Union.
Hartmut Krafft, Chantal Bélorgey, Gudrun Szalay

Nat Rev Drug Discov· May 2012

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Hartmut krafft. Interview by Bethan Hughes.
Hartmut Krafft

Nat Rev Drug Discov· June 2010

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Good clinical practice in the European Union.
Immanuel Barth, Hartmut Krafft, Gabriele Weber, Brigitte Keller-Stanislawski, Klaus Cichutek

Hum Gene Ther· May 2008

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