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Overall it has its own read, though

1 Congress does not have the institutional capacity to monitor and respond to ongoing innovations in product design (especially those purporting to reduce exposure to tobacco-related toxins), or to changes in marketing or patterns of consumption, whereas FDA personnel are well-positioned to gather the necessary information and to make evidence-based scientific judgments about the likely public health consequences of alternative regulatory approaches

Part of it is these things are so new and they're happening so fast it is so difficult, said Goldstein

[183] The prosecution's first witness, Katie Blackwell, testified for three days about the department's training and policies regarding use of force