Hart Clinical Consultants (HCC) is a Specialty Clinical Research Organization (CRO), expertly staffed, providing business partners with unparalleled world-class clinical and research support services through all trial phases.
Proper use of novel medical devices is imperative for patient safety and critical for meeting performance endpoints.
Source data verification is the industry standard for ensuring your clinical trial results in data of the utmost integrity.
Juggling too many balls in your clinical trial? Project management and Site Management services keep your project on track.
An experienced data management team can handle your clinical data with efficiency to bring exceptional value from the research lab to the bedside.
The Clinical Events Committee, or CEC, improves the validity of study safety endpoint data.
Being proactively prepared for an inspection of your clinical study ultimately helps streamline the path to your regulatory submission and approval.