Biotech Leaders
FDA & ICH
What are the signature requirements for translated informed consent documents?
Blog Posts
Series: Ask the IRB & IBC Experts
Can participants be reconsented over the phone when an ICF is updated?
Blog Posts
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
Stump the Experts: Patient Recruitment Q&A
Videos
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