Insights
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
Get under the hood while the trial is running: Identify and rectify data problems before it’s too late
Blog Posts
WCG Introduces Unique Benchmarking Solution for Medical Device Companies
News
Regulatory Compliance