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21 CFP Part 11 (Electronic Records & Signatures)
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Obtaining Approval for Clinical Trials in US & EU for Regulatory Professionals
GCP00A2
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$
845.00
Clinical Research Associate (CRA) Professional Certification Program
GCP00A
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$
695.00
Computer System Validation for Professionals
VAL00S2
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$
645.00
Pharmaceutical Sales & Marketing Compliance Professional Certification
SAMPRO
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$
399.00
DIGR-ACT® Solution: Critical Thinking Skills – Including Root Cause Analysis & CAPA
CP001a
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$
359.00
Pharmacokinetics and Pharmacodynamics for Professionals
AV01A
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$
245.00
Validation & Compliance: Commercial-off-the-shelf (COTS), Software-as-a-service (SaaS) and Cloud Systems
CSA-301
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$
225.00
Compliance with Regulation 21 CFR Part 11 (Electronic Records and Electronic Signatures)
ESR01A
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$
225.00
Regulatory Affairs: The Biologics License Application (BLA) for Marketing Approval in the USA
SUB15
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$
225.00
Regulatory Affairs: Variations to Marketing Authorizations in Europe
PRA22
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$
225.00
Regulatory Affairs: Submitting a New Drug Application (NDA) to Obtain Approval to Market in the USA
PRA07
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225.00
Regulatory Affairs: How to Gain Approval to Market Generic Drugs in the USA
PRA06
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