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IPRC Services
- Bioavailability / Bioequivalence
Studies:-
- Institutional Review Board (IRB).
- Good Clinical Practice (GCP).
- Good Laboratory Practice (GLP).
- Quality Assurance Unit (QAU). -
- Comprehensive protocol and CRF design.
- Assay method development and validation.
- Drug analysis in biological matrices.
- Full statistical data analysis.
- Report and literature review.
- Timely reports for regulatory submission.
IPRC conducts its clinical trials in reliable
and sophisticated hospitals in Jordan according to a carefully designed
study protocol. A special wing/unit is assigned for the conduct
of these studies. All Utilities of the hospital such as the emergency
unit, the nutritional unit, the Intensive Care Unit and the medical
laboratories are available to IPRC. We Provide Timely, Accurate
and Affordable Results:- Our clinical staff is fully trained in
the performance of clinical trials. Our sample collections are on
exact schedule, in strict compliance with the protocol for each
study. Our highly accurate data collection and management system
provides a clean, logical paper trial and source documents
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