Blinded Vs. Unblinded Clinical Study In Oncology: Overcoming Bias, Safety Challenges, & Regulatory Demands
One of the primary concerns when considering a clinical study in oncology is how to ensure that the findings are reliable, objective, and acceptable to the regulators. The solution usually involves blinding, and eventually, when necessary, unblinding. Blinding limits the possibility of bias by keeping patients and researchers unaware of the treatment they receive or […]
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