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Dr. Cecilia Wanjala
Head of Regulatory, Quality and Planning

Main areas of responsibility include developing the Regulatory strategy for the facility and for the HPTs that are to be manufactured at the Institute, and embedding a quality management system across the organisation. In addition, Dr. Wanjala’s responsibilities include supporting the CEO / DG in developing the corporate strategy for the organisation.
Dr. Wanjala has been seconded from Kenya Medical Research Institute.