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At
the heart of our program is our commitment to full-service,
organized study management. From contract award to study
closure, a dedicated team is responsible for oversight
of each study and delivery of accurate data files. Our
staff is thoroughly trained in protocol management,
laboratory processes and client relations.
Project Managers develop detailed project plans at project
onset, with all tasks, timelines and milestones delineated.
They monitor these plans and document progress to share
with the sponsor, and to ensure strict adherence to
protocol deadlines.
We proactively work with investigator sites to expedite
every aspect of subject data collection, sample logistics
and reporting. Our team provides investigator sites
with training in the use of all clinical supplies and
materials.
Quality and documentation are critical to the success
of the study and are fundamental in our project management.
We confirm that all necessary validation and quality
control procedures are in place and monitored throughout
the trial.
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Protocol-specific data entry
restrictions promote use of proper data formats |
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Customized data validation
checks for clean data at point of entry |
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Dedicated staff for efficient
communication and support of your protocol |
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Protocol-specific requirements
implemented in testing, reporting and specimen
storage systems |
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Customized Investigator
manuals, requisition forms and shipping instructions |
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Protocol-specific collection
kits -- designed, manufactured and shipped directly
to investigator sites |
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Nationwide logistical network
of trained couriers for specimen pick up and shipment |
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