RESEARCH Australia has made a
submission to the National Health
and Medical Research Council’s
(NHMRC) consultation on good
practice process for clinical trials,
saying the keys to improving clinical
trial governance were uniform
and ‘trial appropriate’ approaches
across all jurisdictions, and the
greater use and acceptance of
multi-site ethical approvals.
The state and territory
governments needed to be
engaged in the reform process,
which should be appropriate to
the nature of the clinical trial, for
instance, non-drug trials were
lower risk typically but paediatric
trials had specific requirements,
Research Australia said.
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