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MedClin Research provides full site management services for pharmaceutical and medical device studies. The central office provides comprehensive administration for all sites including:
All research sites have the following features:
The end result is a highly organized and efficient process to collect and record accurate, quality data. The research physicians have been chosen for their experience and professionalism. These physicians have been asked to join the MedClin network due to their history of entering quality research patients, cooperating with the research team, and providing exceptional care to their patients. The central administration and study coordination are performed by highly experienced clinical research associates. Many of the CRAs have been monitors for the pharmaceutical industry. The experience of the CRAs contributes to the high standards achieved by MedClin research. MedClin research is staffed with highly experienced personnel - some members have been involved in clinical research for more than twenty years. Many of the research support staff have experience as both coordinators and monitors. As such, the needs of the sponsors are well understood and every endeavor is made to satisfy those requirements. An in-house quality assurance program is in place to ensure that the data
collected is of the highest standard. |
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