Sponsored by the MGH Division of Clinical Research, the Partners Human Research Office (IRB) and the Partners Human Research Quality Improvement Program (QI).
Speaker: Daniel Jones, QA/QI Speacialist
Isabel Chico-Calero, QI Program Regulatory Specialist
This series is designed for all researchers and study staff who are submitting materials to the IRB and planning to conduct a study. The first lecture in each session will elucidate ethical and regulatory aspects of human subjects research and provide guidance on what information the IRB needs for review. The second session will be presented by the QI Program and will provide additional guidance, tools and practical tips on how to adhere to these regulations in your research. Please note: Attendees may choose to attend all sessions or can attend whichever sessions are pertinent to their learning needs.
This session is limited to 25 participants to facilitate interaction.
Registration is required.Please contact dcredu@partners.org with any questions.
Programs: Clinical Research Investigator Beginner Clinical Research Coordinator
Categories: Clinical Research Ethical Oversight Research Quality Improvement
Sponsor: MGH Division of Clinical Research
Modules
| IRB and QI Roundtable Series - Session I - Part II: Study Start-Up |
Past Offerings
| QI Roundtable - Study Start-Up | Sept. 22, 2016 |
| QI Roundtable - Study Start-Up | Sept. 28, 2017 |