§ Katalog
Eğitim Programları
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Good Clinical Practice (GCP) E6(R3) Training — ICH-Based
ICH E6(R3) GCP training based on TransCelerate Minimum Criteria v3.0. 16 modules, 25 hours. For investigators and site personnel.
6 modül
25 sa
EN
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Clinical Research Associate (CRA) Certification Program — English
Comprehensive CRA training covering monitoring, SDV, RBQM, site management, and ACRP-CCRA/SOCRA-CCRP exam preparation. Based on ICH E6(R3), FDA Risk-Based Monitoring.
10 modül
11 sa 40 dk
EN
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Clinical Research Monitor (CRA) Training Program — English
12-module CRA/Monitor training: site visits, SDV, RBQM, IP, safety, CAPA, reports, inspection prep. Based on ICH E6(R3), FDA RBM, ACRP CCRA.
12 modül
10 sa
EN
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