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- 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