Ended: Sept. 14, 2017
IRB Roundtable: New Submissions
Speakers: Sheldon Ratnofsky, Human Research Specialist
Learn how the Administrative Chairs (voting members of the IRB) review and consider ethical, scientific and regulatory aspects of human subjects research during full board review of new protocols. The Administrative Chairs will explain the commonly encountered Federal Regulations and how they can be addressed in your submission, as well as common deficiencies in protocol summaries.
This session is limited to 25 participants to facilitate interaction. Registration is required.
Please contact email@example.com with any questions.
Programs: Clinical Research Investigator Beginner Clinical Research Coordinator Experienced Clinical Research Coordinator
Sponsor: MGH Division of Clinical Research
Sept. 14, 2017
|12 PM – 1 PM||
Garrod/Mendel, Floor 2, Simches Research Center