Fundamentals of Clinical Research Monitoring

Industry's Most Comprehensive Course on Clinical Research Monitoring

Interactive lecture and hands-on workshop training methods will provide you with the tools to design and manage clinical studies.

WHAT YOU WILL LEARN

·          Good Clinical Practices (GCP) 

·          Regulatory requirements for clinical research 

·          Clinical research methodology and its role in drug development 

·          CRA's role in clinical research 

·          Monitoring clinical trials to ensure valid and useful study data 

·          Investigator selection and evaluation 

·          FDA audits 

·          Basic HIPPA requirements 

·          Basic protocol development