Adverse Event Reporting and Post-Marketing Activities, BPHE 5725P
Addresses the regulations governing reporting of adverse events in clinical trials and post-marketing surveillance regulations as required by the FDA.
Applied Clinical Trials, BPHE 6352P
In-depth discussion of protocol management and patient management processes. Students are expected to apply these concepts in simulated clinical trial situations.
Biomedical Informatics for Clinical Trials Management BINF 5075P
Focused discussion of the principles and techniques of biomedical informatics as related to clinical trials.
Clinical Trials Overview:
Methodology and Practice, BPHE 5310P
Basic principles of good study design and implementation.
Cultural Diversity in Clinical Trials, BPHG 5800G
This course promotes understanding of the effects of disparities in clinical trials and pharmacological management in global populations.
Ethical Issues in Health Care Practice, NUTR 6505
Bioethics, malpractice, experimentation and other critical issues are examined in a framework of multicultural diversity.
Food and Drug Law, BPHE 5100P
Historical review of events shaping food and drug law as well as an indepth exploration of current legal and regulatory requirements
Microarrays in Clinical Trials, BINF 5225P
An indepth introduction to the use of microarray technology, chip design, and protocol development in large-scale data collection and mining
Principles of Subject Recruitment and Retention, BPHE 6985P
Training in the modern principles and techniques used in evidence-based planning of subject identification, qualification, and enrollment.
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