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Clinical Trials for Sponsors and CROs
Clinical Trials for Sponsors and CROs
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21 CFP Part 11 (Electronic Records & Signatures)
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Clinical Trials Management (US & EU) Professional Certification Program
GCP00A1
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$
895.00
Obtaining Approval for Clinical Trials in US & EU for Regulatory Professionals
GCP00A2
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$
225.00
Clinical Trials: How to Gain Authorization for Clinical Research Under the EU Clinical Trials Regulation
CT11
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$
225.00
Clinical Trials: The Investigational New Drug Application (IND) to Conduct FDA-regulated Clinical Trials
GCP007
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$
225.00
Clinical Trials: Preparing for an Audit or Inspection
GCP006
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$
225.00
Clinical Trials: Preparation and Design
GCP002
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$
199.00
Regulatory Requirements for Clinical Trials in Europe (Directive to Regulation)
CP018a
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$
199.00
Overview of 21 CFR Part 54 Financial Disclosure & Part 11 Electronic Data Signatures
CP016a
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199.00
Overview of 21 CFR Part 312 Investigational New Drug Application (IND) and 21 CFR 314 Application for FDA Approval to Market a New Drug (NDA)
CP015a
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199.00
Structure and Content of Clinical Study Reports (ICH E3)
CP013a
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199.00
Clinical Safety Data Management: Definitions and Standards for Expedited Reporting (ICH E2A)
CP012a
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199.00
CRO Oversight
CP007a
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