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Regulatory Writing
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15
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Title
Credit(s)
1
Clinical Study Report Development Pt 2
(6 votes)
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1.0 CE
2
Clinical Trial Transparency: What you need to know about European Medicines Agency Policy 0070
(0 votes)
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|
1.0 CE
3
CORE Reference: A Medical Writer’s Guide to Preparing CSRs in an Evolving Context
(9 votes)
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|
1.0 CE
4
Creating a Highly Effective Road Map for Clinical Research: Authoring the Clinical Study Protocol
(1 votes)
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|
1.0 CE
5
Differences and Similarities Between Publication and Regulatory Medical Writing
(0 votes)
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|
1.0 CE
6
Effective Project Management for Regulatory Documents During the Document Process
(1 votes)
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|
1.0 CE
7
Effective Project Management for Regulatory Documents Prior to the Document Process
(0 votes)
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|
1.0 CE
8
Effective Project Management: Paving the Path to Successful Regulatory Documents
(3 votes)
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|
3.0 CE
9
Invisible Ink: Writing Considerations for a Transparent World
Member $20 | Nonmember $55
(1 votes)
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|
1.0 CE
10
Managing Various Components of the Authoring and Publishing Stages of an Application
(0 votes)
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|
1.0 CE
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