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German ePharma Day 2014

Risk Based Monitoring in Clinical Trials - A new approach for managing risk-bearing activities throughout the design, conduct, evaluation and reporting of clinical trials. Conduction of the 100% of Source Data Verification (SDV) at every investigational site or the implementation of the current common practices in trial monitoring are not the way to assure the quality of data in a clinical trial and are acknowledged to be time and costs consuming.
  • Risk Based Monitoring in Clinical Trials - A new approach for managing risk-bearing activities throughout the design, conduct, evaluation and reporting of clinical trials. Conduction of the 100% of Source Data Verification (SDV) at every investigational site or the implementation of the current common practices in trial monitoring are not the way to assure the quality of data in a clinical trial and are acknowledged to be time and costs consuming.
    50.0324676 8.5922099
Wann 26.06.2014
von 09:00 bis 18:00
Veranstaltungsort InterCity Frankfurt Airport Hotel
Stadt Frankfurt/Main
Kontaktname
Kontakttelefon +393388422561
Zielgruppe The conference is addressed to all the Clinical Research Professionals with a deep interest in the implementation of a Risk Based Monitoring approach, belonging to the following departments:
• Clinical Research and Development
• Quality Assurance
• Pharmacovigilance
• Clinical Operations
• Statistics and Data Management
• Information Technology
from Pharmaceutical and Biotechnology companies, Clinical Research Organizations, Academic Centres, Hospital Centres, and Clinical Technology companies.
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