Med/Sci
FDA & ICH
What are the IRB submission requirements for observational studies?
Blog Posts
Questions on regulations for process development and purchased human cells
Blog Posts
Regulatory Compliance
What training documentation is required for conducting clinical research studies?
Blog Posts
What are ethical considerations for a trial with a pre-study washout period?
Blog Posts
Virtual Clinical Trials: Best Practices in Moving Toward a Patient-Centric Research Model
Whitepapers
Regulatory Compliance
How to resolve irregularities in the documentation of informed consent?
Blog Posts
Ethics in Clinical Research
Can the IRB approve reimbursement of copays for routine costs in a clinical trial?
Blog Posts
Regulatory Compliance
Is IRB review required for survey results that may be published?
Blog Posts
Clinical Endpoints
Podcast: The Role of Expert Committees in Clinical Research with guest Jonathan Seltzer, MD, MBA, MA, FACC
Podcasts
Clinical Endpoints