Research Ethics and Good Clinical Practice Workshop

Cairo, Egypt
8-10 January 2009

Participating Institutes: Cairo University, National Cancer Institute, and Theodor Bilharz Research Institute

• Agenda (PDF)

• Faculty Profiles (PPT)

• Audio Powerpoint Presentations
  All files in flash (swf) format.
  
  

  • History and Principles of Research Ethics – Hany Sleem

  • Criteria for Review of Research: Ethical Requirements – Nahed Moustafa

  • Overview of Clinical Trials – Hala Mansour

  • Distinction Between Research and Clinical Practice – Henry Silverman

  • Vulnerable Subjects – Nahed Moustafa

  • Introduction to Good Clinical Practice - Isabelle Nakhla

  • Investigator's Responsibilities – Mohamed Adel

  • Essential Documents – Sahar Ebrahim

  • Screening and Enrollment – Hala Mansour

  • Informed Consent – Hany Sleem

  • Safety in Clinical Trials: Adverse Events and DSMB – Azza Saleh

  • Role and Functions of Research Ethics Committees – Azza Saleh

  • In Trial Procedures/Source Documents/Data Collection – Wesam Masoud

  • Analysis of Risks and Benefits – Nahed Moustafa

  • Principles of Quality Assurance – Radi Hammad

  • Research Misconduct – Henry Silverman

Printer friendly    Email this page