CLEAN : Concerns as India prepares to roll out home-grown vaccine

The transcript begins with a series of disjointed and random phrases, followed by a discussion on the importance of informed consent in clinical trials. It highlights that no hospital or part of the world can conduct trials without patient consent, as per clinical practices. The transcript concludes with concerns about the conduct of these trials, suggesting a need to investigate potential impacts on science and data.

How might adverse side effects impact the perception of a clinical trial?

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What steps should be taken if there are clear misses in trial conduct?

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