Ethics in Clinical Research
Clinical Trial Safety
Safeguarding Participant Rights and Safety Requires Collaboration: Exploring the Duties of Sponsors, Sites and IRBs
Blog Posts
Cell & Gene Therapy
Why Biotech Sponsors Need Outside Support: IRB, IBC, DMCs and EACs
Whitepapers
Ethics in Clinical Research
Research and Cannabis: Ethical Research in a Changing Regulatory Landscape
Whitepapers
Ethics in Clinical Research
What Can Institutions with Local IRBs Do to Prepare for the Proposed FDA Single IRB Mandate?
Whitepapers
Ethics in Clinical Research
Caregivers as Research Participants
Blog Posts
Ethics in Clinical Research
Reviewing the FDA’s Proposed Informed Consent Rule Changes
Whitepapers
Ethics in Clinical Research
Employees as Research Participants
Blog Posts
Ethics in Clinical Research
Understanding the FDA’s new proposed regulations on human subject research and their impact on your clinical trial plans
Videos
Ethics in Clinical Research
Should a Protocol Amendment be Submitted in Advance of Consent Form Changes?
Blog Posts
Ethics in Clinical Research