New FDA Guidance on the Use of Multiple Endpoints in Clinical Trials
The U.S. Food and Drug Administration (FDA) issued a new final guidance, Multiple Endpoints in Clinical Trials Guidance for Industry. As the number of endpoints...
Read The ArticleThe U.S. Food and Drug Administration (FDA) issued a new final guidance, Multiple Endpoints in Clinical Trials Guidance for Industry. As the number of endpoints...
Read The ArticleAs part of their commitment to to supporting ethically conducted, high quality research, the National Institutes of Health (NIH) has released a new webpage, Animals...
Read The ArticleThe AAMC (Association of American Medical Colleges) and COGR (Council on Governmental Relations) have issued a response to NOT-AT-22-026, the NIH’s request for information, Investigators’...
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Read The ArticleThe World Health Organization (WHO) has released a draft guidance titled, WHO International Clinical Trials Registry Platform (ICTRP) guidance for reporting summary results in clinical...
Read The ArticleAs a research administrator, challenges can present themselves in many different forms. These challenges can range from accounting discrepancies to facilities issues, and regulatory burdens....
Read The ArticleSeason 1 – Episode 21: Student Engagement: Colleges and Universities Student engagement is a vital part of the college and university experience, ranging from activities...
Read The ArticleOverview: Clinical Trial Roles and Responsibilities A clinical monitoring plan is a carefully crafted template for each unique clinical study to guide the participant and...
Read The Article“What CITI Program is Reading” is our weekly blog series which highlights news articles curated by our staff and relevant to research, higher education, healthcare,...
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