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21 CFP Part 11 (Electronic Records & Signatures)
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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
Investigator Initiated Clinical Trials
CP011a
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$
199.00
ISO 14155:2020 Medical Device Standard
CP008a
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$
199.00
CRO Oversight
CP007a
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199.00
Corrective and Preventive Action (CAPA) Process Planning for Clinical Research Professionals
CP006a
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$
199.00
Good Documentation Practices and ALCOA-C
CP005a
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$
199.00
Overview of ICH E8(R1): General Considerations for Clinical Studies Guideline
CP019a
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$
199.00
ICH E6(R2) GCP Training for Investigator Site Personnel
CP004a
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199.00
GCP Refresher Training for the Experienced Professional
CP003a
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$
199.00
GCP Training: ICH E6(R2) – (Refresher Training for Novice)
CP002a
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199.00
cGMP: Introduction to Good Manufacturing Practice (GMP)
GMP01
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