Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Series: Ask the IRB & IBC Experts
Is it possible to make a PI’s name or institution confidential on a consent form?
Blog PostsNIH Launches NExTRAC to Advise on Emerging Biotechnologies
Blog PostsWCG’s Clinical Research Trends & Insights for 2020
Blog PostsHow to Maximize ROI by Implementing a Holistic Recruitment Strategy
Blog Posts
Series: Ask the IRB & IBC Experts
What are the Blood Draw Guidelines for Phase 1 Clinical Trials?
Blog PostsQuestions on Using Generic Recruitment Flyers at Clinical Trial Sites
Blog Posts
Ethics in Clinical Research
An Overview of the Recent SACHRP Recommendations Around Payments in Clinical Research
Blog Posts
Clinical Endpoints
Creating Scientific Rigor in Medical Device Trials
Blog Posts
Regulatory Compliance
Guidance on genomic research with deceased patients
Blog Posts
Clinical Endpoints