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Developing Data Collection Tools & Conducting Self-Audits (for non-FDA regulated studies)
September 18 @ 10:00 am - 11:30 am
This presentation is geared toward non-FDA regulated research studies. The presenters will describe tips and tricks to consider when developing data collection tools, and attendees will take part in an interactive workshop in which they will learn and apply self-audit principles to mock subject charts and records.
Post-Approval Monitors from the Office of Research Compliance:
Travis Doran, Peter Johnson, and Emily Putman-Buehler
Emily Putman-Buehler, firstname.lastname@example.org