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Pharmaceutical Regulatory Affairs
Pharmaceutical Regulatory Affairs
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21 CFP Part 11 (Electronic Records & Signatures)
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Regulatory Affairs: Essentials of Monoclonal Antibodies
PRA24
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145.00
Regulatory Affairs: The European Centralized Procedure (CP)
PRA20
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145.00
Regulatory Affairs: Preparing Submissions in the Common Technical Document (CTD) Format
PRA03
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145.00
Regulatory Affairs: Orphan Drug Application – EU and US
PRA02
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Regulatory Affairs: The Regulatory Pathway to Licensing Follow-on Biologics (Biosimilars) in the USA
PRA08
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