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DNA adduct burden and tobacco carcinogenesis
The FDA has not started to conduct pre-market reviews, pushing the deadline back to August 2021 with the rationale that it, will allow companies to develop higher quality, more complete applications. The FDAs current approach appears to be to talk big but do little, while deferring and delaying implementation of effective regulation
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(2019) Genotoxic and carcinogenic potential of compounds associated with electronic cigarettes: a systematic review
