Showing results for IRB

Congratulations, You Have Unlocked the Webinar
Working with Your IRB This webinar provides a discussion of effective communication strategies for students and faculty to work with their IRB. The w...
On Research Podcast - Updated Research Misconduct Final Rule
Season 2 - Episode 11 - Updated Research Misconduct Final Rule This episode discusses the updated research misconduct final rule. ...
Explore New Insights from OHRP's Recent Webinar Recordings
The Office for Human Research Protections (OHRP) has recently made three impactful webinar recordings available, offering invaluable insights into som...
Communicating with Subjects
Provides guidance to IRB administrators on circumstances and procedures that should be considered when communicating with subjects before, during, or ...
Communicating with Subjects
Provides guidance to IRB administrators on circumstances and procedures that should be considered when communicating with subjects before, during, or ...
On Tech Ethics Podcast - Modernizing Clinical Trials with ICH E6(R3)
Season 1 - Episode 32 - Modernizing Clinical Trials with ICH E6(R3) Discusses the updated International Council for Harmonisation (ICH) Guideline for...
Social Media Research
With billions of users worldwide, social media is integral to modern life, and its significance continues to grow. For researchers, social media has p...
Clinical Research Coordinator (CRC) Foundations
The CRC Foundations course provides clinical research professionals with basic training tailored to the CRC’s fundamental role in the conduct of cli...
GDPR for Research and Higher Ed
The General Data Protection Regulation (GDPR) protects the personal data and privacy of individuals in the European Economic Area (EEA), including all...
Clinical Trial Agreements (CTAs)
CTAs are one of several key documents that govern the conduct of clinical trials. A CTA serves as a legally binding contract between a sponsor, site, ...
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