IPPCR 2018: Legal Issues in Clinical Research
The Introduction to the Principles and Practice of Clinical Research (IPPCR) is a course to train participants on how to effectively conduct clinical research. The course focuses on the spectrum of clinical research and the research process by highlighting epidemiologic methods, study design, protocol preparation, patient monitoring, quality assurance, and Food and Drug Administration (FDA) issues. For more information go to https://ocr.od.nih.gov/courses/ippcr.... Carrie Kennedy. R.N., Esq.
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IPPCR 2019 Issues in Randomization Part 1 of 4
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IPPCR 2016: Ethical Principles in Clinical Research
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Clinical Trials Overview: Phrases and Phases of a Clinical Trials
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IPPCR 2015: Design of Epidemiologic Studies
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Ethical Issues in Clinical Trials (Lecture-49)
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Electronic Documents and Electronic Data in Clinical Research
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IPPCR 2015: Conceptual Approach to Survival Analysis
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IPPCR 2015: Overview of Clinical Study Design
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The Principles of the Belmont Report and the Ethics of Human Research
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What is a Clinical Trial Management System (CTMS)?
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IPPCR 2015: Issues in Randomization
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Ethics in Adult Clinical Pharmacology with Dr. Ezekiel J. Emanuel
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Simplifying Informed Consent (with OHRP)
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Understanding Clinical Trials in Cancer Care
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Adverse Event and Safety Monitoring in Clinical Trials
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Aging and Inquiry: Partnering with Older Adults in Research
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Good Clinical Practice
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SOCRA Review: Investigator Roles and Responsibilities in Clinical Research
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IPPCR: Quality Management in Clinical Research
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