German ePharma Day 2014
14.04.2014 15:14
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.
Termindetails
Wann
26.06.2014
von 09:00 bis 18:00
von 09:00 bis 18:00
Wo
Frankfurt/Main
Name
Kontakttelefon
+393388422561
Teilnehmer
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.
• 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.
