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Complying with the HIPAA Privacy Rule in Research
Total CE's 20 Qty:
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Investigator Training Program
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A Coordinator's Guide to Conducting Clinical Research
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Seminar Library
GCP & IND - Sponsor
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GCP & Conduct & Supervision - Investigator
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GCP & Monitoring & Managing - Sponsor
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Overview of Medicinal Product Development
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GCP & Protecting Subjects - Sponsor
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Seminar Library
ICH E6 GCP Guidelines
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GCP & Review and Approval - IRB
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GCP & Obligations and Methods - Monitor
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HIPAA-M
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Clinical Trial Development
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Clinical Trial Management
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Essentials of Clinical Data Management
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Good Clinical Practices - PH
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Good Clinical Practices - Device
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Good Clinical Practices - Drug
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GCP from the Investigator’s Perspective
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