RESPONSIBLE CONDUCT OF RESEARCH

1
RESPONSIBLE CONDUCT OF RESEARCH RB-3 First Floor
Conference Room Stewart A. Laidlaw, PhD
Director, Compliance Office, LA BioMed
W i n t e r 2 0 0 8 P r o g r a m S c h e d
u l e
Core Unit 2 1/23 On Being a Scientist The
Ethical Conduct of Research Wednesday
400-500pm This session will cover the
responsibility of a scientist with regard to
conduct of research. Various areas of misconduct,
including falsification, fabrication and
plagiarism will be reviewed. The session will
also review the regulatory response to instances
of scientific misconduct, the Institutional
position, including its assurance, and the role
of the Ethical Standards in Research Committee.

• Core Unit 1
• 1/16 Protecting Human Study Volunteers
• Wednesday 400-530PM
• Historical Perspective
• Ethical Response
• Regulatory Response
• Institutional Review Boards
• Informed Consent
• Applying and interpreting the regulations
• Special protections for vulnerable subjects

G e n e r a l C l i n i c a l R e s e a r c h
C e n t e r Los Angeles Biomedical Research
Institute at Harbor-UCLA Medical Center
Core Unit 4 2/6 Case Discussions Wednesday
400-500pm Course participants will discuss
specific scenarios and the ethical issues
involved. The format will be round table with a
discussion leader to guide the discussion.

• Core Unit 3
• 1/30 Practical Issues in the Conduct of Research
• Wednesday 400-500pm
• Data acquisition, management, sharing and
  ownership
• Mentor/trainee responsibilities
• Publication practices and responsible authorship
• Peer review
• Collaborative science

Contact the GCRC office to register!
gcrcinfo_at_labiomed.org