Recently, there have been updates to ClinicalTrials.gov enforcement and various initiatives to drive transparency. Institutions are challenged to build robust compliance programs and individuals must...
Read The ArticleThis webinar covers a brief overview of the regulations, important timelines to follow, agency-specific variances, and a range of compliance mechanisms. It also covers the...
Read The ArticleThis webinar discusses how to improve the informed consent process for subjects enrolling in clinical research. It focuses on the process used to deliver information...
Read The ArticleWith the transition to remote work due to the COVID-19 pandemic, research teams, Institutional Review Boards (IRBs), and others supporting human research have worked to...
Read The ArticleThis webinar explores critical points for individuals seeking to write their first National Institutes of Health (NIH) R01 application. It includes a brief overview of...
Read The ArticleThis course includes both the CRC Foundations and CRC Advanced courses to provide all your CRC-focused training in one comprehensive package. The courses cover information that...
Read The ArticleThis course covers the essential elements of IACUC administration, including a review of the animal care and use regulations and guidelines, IACUC functions, the IACUC...
Read The ArticleEC Refresher begins with a basic review of export compliance. Other modules in the EC Refresher course discuss export compliance issues and concepts that can...
Read The ArticleReviews the important role of the biomedical investigator (also referred to as the clinical investigator or principal investigator [PI]) in a clinical investigation that complies...
Read The ArticleSemiannual Evaluations In Depth complements and expands upon the basic regulatory elements covered in the Essentials for IACUC Members course. It provides more in-depth information...
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