Bioavailability Unit
Overview:
aims to carry out bio-availability and bio-parity studies of generic preparations. In addition to studying the rate of melting of these preparations in accordance with the latest regional and international standards and requirements in order to contribute to the advancement of the local pharmaceutical industry and to strengthen scientific research in the pharmaceutical industry and to achieve the highest levels of quality and excellence, these studies are conducted in accordance with the rules of good laboratory practice (GLP) and good clinical practice (GCP).
Unit capabilities
The unit includes a number of researchers and faculty members experienced in this field in addition to the use of college staff with experience in the field of the work of the unit.
The unit includes many advanced devices and modern technologies, including separation devices, chromatograph analysis, mass spectrometers as well as other basic laboratory devices.
The Unit provides services and conducts research in the:
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Use analysis methods to extract and determine the level of medicines in biological fluids and study their pharmacological mobility, especially drugs with a critical therapeutic rate.
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Study of the bioavailability of new pharmaceutical formulations that have been prepared using modern technologies in order to reduce their side effects or to improve the rate of their absorption in the body.
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Holding training courses in chromatographic methods and pharmacokinetic measurements in biological fluids.
Contact Info:
Bioavailability Unit Supervisor:
Dr.Mohammad Altamimi
