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21
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34
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Title
Credit(s)
21
CORE Reference: A Medical Writer’s Guide to Preparing CSRs in an Evolving Context
(9 votes)
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1.0 CE
22
Clinical Trial Transparency: What you need to know about European Medicines Agency Policy 0070
(0 votes)
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|
1.0 CE
23
When a Guide Becomes a Rule: The Food and Drug Administration’s Rulemaking Authority and its Impact on Submissions Documents
(0 votes)
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|
1.0 CE
24
Effective Project Management for Regulatory Documents Prior to the Document Process
(0 votes)
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|
1.0 CE
25
Effective Project Management for Regulatory Documents During the Document Process
(1 votes)
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|
1.0 CE
26
Effective Project Management: Paving the Path to Successful Regulatory Documents
(3 votes)
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|
3.0 CE
27
Clinical Study Report Development Pt 1
(11 votes)
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|
1.0 CE
28
Introduction to Health Economics and Outcomes Research (HEOR) for Writing Professionals
(2 votes)
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|
1.0 CE
29
TransCelerate’s Common Protocol Template (CPT) and the Technology-Enabled Addition
(0 votes)
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|
1.0 CE
30
Metrics: Proving Our Value
(1 votes)
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|
1.0 CE
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