B18 - "Let it Go": What Should Be Exempt and How to Limit IRB Review of These Studies (Including Those With Sensitive Data) Talks and Presentations 2017 AER Conference 11/06/2017
B16 - Mastering Master Agreements: When Are Broad-Based Standardized Agreements Beneficial to Research Collaborations? Talks and Presentations 2017 AER Conference 11/06/2017
B14 - Tips and Tools for Implementing Single IRB Review Talks and Presentations 2017 AER Conference 11/06/2017
B12 - Back to Basics: Does My Project Fall Within the Scope of the Revised Common Rule, or Is it Exempt? Talks and Presentations 2017 AER Conference 11/06/2017
A21 - IRB Review of Big Data Research Talks and Presentations 2017 AER Conference 11/06/2017
A14 - Considerations When Transitioning to the Revised Common Rule Talks and Presentations 2017 AER Conference 11/06/2017
A8 - The Use of Real-World Evidence to Support Regulatory Decision-Making for Medical Devices Talks and Presentations 2017 AER Conference 11/06/2017
A5 - Facilitating Informed Consent in Light of the Revised Common Rule Talks and Presentations 2017 AER Conference 11/06/2017
Aligning SOPs and New Electronic Systems for a Successful Implementation Webinars 09/13/2018
EU General Data Protection Regulations: What US Research Institutions Need to Know Webinars 04/25/2018
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