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Delta’s clinical
research practice concentrates on ensuring the
integrity of the clinical trial and safety of
study participants. Clinical Research requires
a depth and breadth of knowledge to ensure that
Good Clinical Practices and study protocols are
followed. Moreover,
such knowledge allows us to verify informed consent
processes, properly document and report adverse
experiences, manage and monitor data & regulatory
issues and numerous other activities required
during the life cycle.
Inexperienced and inappropriate resources not
only delay gaining drug approval, but can also
jeopardize the safety of participants. Delta is
passionate about ensuring the safety and success
of studies by providing resources with significant
experience such as:
• Clinical Study Managers
• Clinical Research Associates
• Clinical Research Coordinators
• Safety Review Nurses
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