SAS Clinical Research TRAINING

Module 1: Introduction to Clinical Research
Module 2: Drug Discovery and Development
Module 3: Bioinformatics and Drug development
Module 4: Introduction of ICH-GCP
Module 5: Roles and Responsibilities of Study Team
Module 6: IRB and IEC
Module 10: Essential documentation in Clinical Research
Module 11: Clinical Trial Process
Module 12: 21 CFR 11
Module 13: Introduction to CDISC
Module 14: Clinical Data Management Process
Module 15: CRF Design
Module 16: EDC ( Electronic Data Capture)
Module 17: MedDRA
Module 18: Pharmacovigilance
Module 19: Adverse Drug Reactions(ADR)
Module 20: EudraVigilance
Module 21: Open Clinica (Comprehensive)
Module 22: Rave(overview)

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