Clinical Trial Directive Web-based Seminars
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From GlobalCompliancePanel
Changes in the EU Medical Device Directives 2010 Modifications and the 2012 Recast of the MDD Directives -Changes in the EU Medi
This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.
Tuesday, March 13, 2012
10: 00 AM PST | 01: 00 PM EST
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Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
...ut in EU obtain the EUDRACT number in accordance with the Clinical Trial Directive requirements
* Start to prepare the outline plan for the study using the work breakdown structure (WBS) technique, outline Gantt chart with estimated timelines for main activities of the study
* Identify possible project risks and uncertainties. Prepare a risk register to handle risks a develop
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