Clinical Research Associate Fundamentals

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Clinical Research Associate Fundamentals

Aim

To ensure the safety and well-being of subjects and patients at all times, clinical trials need to be carried out to the highest quality standards and in accordance with national and international guidelines.

Your benefits

This seminar equips the participants with the necessary skills and knowledge required to effectively monitor the conduct of clinical trials, based on a sound understanding of Good Clinical Practice (ICH-GCP), the legal framework, ethical considerations, and the roles and responsibilities of all parties involved in a trial.