CROs
Ethics in Clinical Research
Save 456 Days in IRB Review With a Seamless, Coordinated Submission Process
Case Studies
Improve Training, Increase Participation, Reduce Redundancy, & Cut Costs: Why Virtual Site Training is the New Norm
Blog Posts
Ethics in Clinical Research
Do parents need to accompany adolescents at each research-related office visit?
Blog Posts
Clinical Trial Operations
Virtual Site Training in Clinical Trials: The New Standard
Videos
Cell & Gene Therapy
Does Human Gene Transfer research at my site require IBC approval?
Blog Posts
Using Predictable and Efficient Data to Take the Risk Out of Site Selection
Whitepapers
Case Study – Feasibility for Type 2 Diabetes Study
Case Studies
FDA & ICH
When should a child assent form be used in a pediatric clinical trial?
Blog Posts
Providing Research Participants with New Information: Is “Re-Consent” Always Necessary?
Whitepapers
Clinical Trial Safety