SCDM Webinars 2011

  • 17 February: What’s New with ePRO Systems: FDA Updates and Regulations
  • 17 March: Adaptive Trial Design – What it Means for the CDM
  • 14 April: Using the CDISC Standards End-to-end in Clinical Trials
  • 19 May: Device Trial Strategies and the CDMs Role in Quality Assurance
  • 23 June: 21 CFR Part 11 for the Clinical Data Manager
  • 22 & 29 September: Biostatistics – What Every Clinical Data Manager Should Know
  • 20 October: Data Integration and the GCDMP: A New chapter in Clinical Data Management
  • 17 November: The Role of Metrics in Clinical Data Management: Tracking Quality and Efficiency