Zhengdai Christiana 正黛 Deng 鄧

Supervising students in the completion and submission dissertation. Providing technical assistance and advice to the student in regards to dissertation structure and design. Acting as examiner at the end of the dissertation process including marking the allocated dissertations. Aiding in the design of the statistical analysis and the interpretation of the results. While qualitative research is acceptable, to ensure that students are fully versed in research methodology at Master's level.

Medical responsibility for all study related medical questions, Medical assessment of projects, Planning and conduct of project-related medical training for the project team, Medical and Safety review of documents developed during a clinical trial, Monitoring of all relevant safety data in the scope of a clinical trial project.

Latest lecture: Drug Development in China (09Feb2011)

Provide oversight of the day-to-day workload in the assessment of adverse event reports to be performed. Database reports validation and quality assurance control. Serve as a mentor/monitor and/or assign mentors/monitors to ensure services and support to adhere to corporate standards, SRM SOPs, project specific guidelines, and that agreed quality standards and SRM timeframes are met.

Master dissertation: Retrospective analysis of adverse event reporting for homeopathic medicines and dietary supplements In the US 2006-2009

Diploma equivalent to MBBS Medical degree.