Overview of Study Start Up Activities for a Clinical Trial at an Investigative Site

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dc.contributor.advisorDr. Patricia Gwirtz
dc.creatorChaudhari, Prianka S.
dc.date.accessioned2019-08-22T21:01:28Z
dc.date.available2019-08-22T21:01:28Z
dc.date.issued2012-11-01
dc.date.submitted2012-11-20T07:40:53-08:00
dc.description.abstractPracticum site, ACRC Trials is a Site Management Organization (SMO) which provides services to the sponsors and Contract Research Organizations (CROs). The main aim of the internship practicum was to describe, analyze and comprehend the study start up activities for a clinical trial at the practicum site. The aim was accomplished by administering survey questionnaire to the staff members, reading study start up Standard Operating Procedures (SOPs) and checklists. If an investigative site optimizes and develops the Standard Operating Procedures (SOPs) for a clinical trial irrespective of type and length of the study then significant time and money can be saved. Saved resources can be used to make an investigative site more efficient in conducting and managing multiple trials.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttps://hdl.handle.net/20.500.12503/29007
dc.language.isoen
dc.provenance.legacyDownloads20105
dc.subjectMedical Pharmacology
dc.subjectMedicine and Health Sciences
dc.subjectOther Medical Sciences
dc.subjectOther Pharmacy and Pharmaceutical Sciences
dc.subjectPharmacy Administration, Policy and Regulation
dc.subjectClinical Trial
dc.subjectClinical Trial Set up
dc.subjectmethodology
dc.subjectdesign
dc.subjectefficiency
dc.subjectsurvey
dc.titleOverview of Study Start Up Activities for a Clinical Trial at an Investigative Site
dc.typeInternship Practicum Report
dc.type.materialtext
thesis.degree.departmentGraduate School of Biomedical Sciences
thesis.degree.disciplineClinical Research Management
thesis.degree.grantorUniversity of North Texas Health Science Center at Fort Worth
thesis.degree.nameMaster of Science

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