Blog Posts
Explore timely perspectives from WCG’s clinical trial operations and scientific leaders.
Get under the hood while the trial is running: Identify and rectify data problems before it’s too late
Blog Posts
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
What are the requirements for submitting protocol deviations?
Blog Posts
Regulatory Compliance
Can we transfer patient data from our CTMS to our parent medical practice?
Blog Posts
Clinical Endpoints
To Mitigate Placebo Response, Test, Train and Control Expectations
Blog Posts
Amendments to the NIH Guidelines: Effects on Human Gene Transfer Research
Blog Posts
What elements of Informed Consent must we include when pre-screening?
Blog Posts
Ethics in Clinical Research