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21 CFP Part 11 (Electronic Records & Signatures)
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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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GCP Training: ICH E6(R2) – (Refresher Training for Novice)
CP002a
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199.00
cGMP: Data Integrity
GMP11
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199.00
cGMP: Pharmaceutical Corrective and Preventive Action (CAPA) – Including Root Cause Analysis
GMP10
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cGMP: Quality Assurance and Quality Control (QA/QC)
GMP09
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cGMP: Packaging Controls
GMP08
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cGMP: Production Controls
GMP07
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cGMP: Contamination Control
GMP06
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cGMP: Documentation and Record Keeping
GMP05
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