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Found 139 events
DUKE SOUTH, ROOM M224 X 02/20/2012 X
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ClinicalTrials.gov

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Investigator Responsibilities

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Human Subjects Research at Duke

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Adverse Events

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Informed Consent

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Informed Consent

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Adverse Events

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ClinicalTrials.gov Introduction

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Study Documentation Regulations and Best Practices

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Human Subjects Research at Duke Overview

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Recruiting Regulations and Best Practices

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Research Databse Design

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Adverse Events

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The Informed Consent Process

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Budget Development and Negotiation Training

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Human Subjects Research at Duke Overview

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Biobanking Best Practices

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Study Documentation Regulations and Best Practices

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Recruiting Regulations and Best Practices

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Human Subjects Research at Duke Overview

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Human Subjects Research at Duke

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