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Good Clinical Practices for the Clinical Research Professional

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Overview 

Gain the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing research studies.

What You Will Learn 

  • Roles and responsibilities of each member of the study team
  • Regulations and guidelines that govern clinical investigations
  • Informed consent elements and processes
  • Successful patient recruitment and retention strategies
  • Adverse event handling and reporting
  • Preparing for audits and the audit process

Who Should Attend 

  • Clinical investigators
  • Clinical research professionals
  • Sub-investigators
  • Study staff

Learning Objectives 

Participants who complete this training should be able to:

  • Identify the roles and responsibilities of each member of the study team including the clinical investigator, sub-investigator, study staff, IRB, and sponsor
  • Apply the regulations and guidelines for conducting safe and effective clinical trials
  • Describe the various processes for informed consent
  • Describe the requirements in reporting adverse events

Contact Information 

Jessica McGrory at +1-215-442-6182 or Jessica.McGrory@diahome.org

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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