Clinical Data Management (CDM) Training Guide

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Purpose of This Training

The purpose of this training is to provide a comprehensive understanding of Clinical Data Management (CDM) and its critical role in clinical research. This training aims to:

  • Build foundational knowledge of CDM processes, terminology, and best practices.

  • Ensure regulatory compliance by covering industry standards such as ICH-GCP, FDA, EMA, and CDISC SDTM.

  • Enhance technical skills in data collection, validation, query management, and database design.

  • Prepare professionals for real-world applications by providing practical examples, case studies, and best practices.

  • Support career growth for individuals transitioning into or advancing within clinical data management.

By the end of this training, participants will have a clear understanding of how CDM supports clinical trials, overall data and trial integrity.

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Purpose of This Training

The purpose of this training is to provide a comprehensive understanding of Clinical Data Management (CDM) and its critical role in clinical research. This training aims to:

  • Build foundational knowledge of CDM processes, terminology, and best practices.

  • Ensure regulatory compliance by covering industry standards such as ICH-GCP, FDA, EMA, and CDISC SDTM.

  • Enhance technical skills in data collection, validation, query management, and database design.

  • Prepare professionals for real-world applications by providing practical examples, case studies, and best practices.

  • Support career growth for individuals transitioning into or advancing within clinical data management.

By the end of this training, participants will have a clear understanding of how CDM supports clinical trials, overall data and trial integrity.

Purpose of This Training

The purpose of this training is to provide a comprehensive understanding of Clinical Data Management (CDM) and its critical role in clinical research. This training aims to:

  • Build foundational knowledge of CDM processes, terminology, and best practices.

  • Ensure regulatory compliance by covering industry standards such as ICH-GCP, FDA, EMA, and CDISC SDTM.

  • Enhance technical skills in data collection, validation, query management, and database design.

  • Prepare professionals for real-world applications by providing practical examples, case studies, and best practices.

  • Support career growth for individuals transitioning into or advancing within clinical data management.

By the end of this training, participants will have a clear understanding of how CDM supports clinical trials, overall data and trial integrity.