Oncology
FDA & ICH
Function over Form: Assessing Different Consent Form Formats
Whitepapers
Ethics in Clinical Research
What Can Institutions with Local IRBs Do to Prepare for a Proposed FDA Single IRB Mandate?
WhitepapersIBC Review
IRB Review
Ethics in Clinical Research
Which comes first – IRB or IBC approval?
Blog Posts
Series: The Future of Clinical Research Sites
The Future of Clinical Research Sites Series Finale: 2022 Year in Review & Look to 2023
Videos
Clinical Trial Operations
The Importance of DMCs: Webinar & Q&A
Videos
Clinical Trial Operations
Complex Clinical Trial Protocol Designs: Impact on the Data Monitoring Committee
Blog Posts
Series: The Future of Clinical Research Sites