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Frühere Veranstaltungen

15.11.17
SZB-Auffrischungskurs: Neuerungen der ICH-GCP-Guideline

15.01.14
Medizinprodukte: Marktzugang - gesetzliche Regelungen
M. Winkel

11.12.13
Anwendungsbeobachtungen und nichtinterventionelle Unbedenklichkeitsprüfungen nach der Zulassung aus regulatorischer Sicht
Dr. Valerie Straßmann, Bundesinstitut für Arzneimittel und Medizinprodukte

13.11.13
Multinational Clinical Trials in Europe and the Voluntary Harmonisation Procedure (VHP)
Dr. Elke Stahl, Bundesinstitut für Arzneimittel und Medizinprodukte

16.10.13
Anforderung an ein Prüfzentrum aus Sicht der Pharmaindustrie
Dr. Klaus Beinhauer, Bayer Health Care, Leverkusen

04.09.13
Vertragsmanagement am Universitätsklinikum Bonn
Mechthild von Normann, GB 2 Finanzwesen und Controlling, UKB

10.07.13
Pharmakotherapie und spezielle Anforderungen an klinische Studien beim alten Patienten
Prof. Dr. Thürmann, Philipp Klee-Institut für Klinische Pharmakologie, Wuppertal

05.06.13
GCP-Inspektionen in Prüfstellen
Guido Scharf, Gesundheitsamt Düsseldorf

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