Trust the Evidence
Trust the Evidence Podcast
Regulatory Data and its Essential role in Assessing Treatment Effects
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Regulatory Data and its Essential role in Assessing Treatment Effects

Discussing, Tamiflu, Comirnaty and Paroxetine Study 329
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Clinical Study Reports (CSRs) are often created as part of the process of submitting applications for new medical treatments to regulators. They are typically very long and, typically, very long, providing much more detail about the methods and the results of a trial.

Several regulators make CSRs publicly available after a drug or vaccine has been approved, improving transparency in the decision-making process.

Studies we discussed

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