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Regulatory Writing
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31
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46
Format
Title
Credit(s)
31
TransCelerate’s Common Protocol Template (CPT) and the Technology-Enabled Addition
(0 votes)
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1.0 CE
32
Introduction to Health Economics and Outcomes Research (HEOR) for Writing Professionals
(2 votes)
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1.0 CE
33
Creating a Highly Effective Road Map for Clinical Research: Authoring the Clinical Study Protocol
(1 votes)
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1.0 CE
34
Effective Project Management: Paving the Path to Successful Regulatory Documents
(3 votes)
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3.0 CE
35
Effective Project Management for Regulatory Documents During the Document Process
(1 votes)
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1.0 CE
36
Effective Project Management for Regulatory Documents Prior to the Document Process
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1.0 CE
37
FIT Series: Hypothesis Testing in Clinical Trials
(2 votes)
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|
.5 CE
38
When a Guide Becomes a Rule: The Food and Drug Administration’s Rulemaking Authority and its Impact on Submissions Documents
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1.0 CE
39
Clinical Trial Transparency: What you need to know about European Medicines Agency Policy 0070
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1.0 CE
40
CORE Reference: A Medical Writer’s Guide to Preparing CSRs in an Evolving Context
(9 votes)
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1.0 CE
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