The Clinical Development Department has the overall
responsibility for clinical and regulatory strategy,
planning and execution and is lead by the Vice-President
of Clinical Development. It is made up of Clinical
Manufacturing function, a Toxicology function, a
Regulatory function, a Clinical Site Management function
and a Safety function. Each of these functions is headed
up by a Director who manages the day-to-day activities.
Additionally, the Clinical Development Department is
responsible for establishing and managing the Clinical
Advisory Board.