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Oversight and Vigilance

Market Vigilance and Oversight of Drugs 253 2. Definition of Significant Deficiencies... [Pg.253]

Market Vigilance and Oversight of Devices 263 Table 12.3 Su mmary of periodic reporting obligations in the US. [Pg.263]

The requirements for market vigilance and oversight in the US are set out in 21 CFR 803, Medical Device Reporting, 21 CFR 806, Reports of Corrections and Removals and 21 CFR 822 Post market Surveillance. [Pg.271]


See other pages where Oversight and Vigilance is mentioned: [Pg.237]    [Pg.238]    [Pg.240]    [Pg.242]    [Pg.244]    [Pg.246]    [Pg.248]    [Pg.250]    [Pg.252]    [Pg.254]    [Pg.256]    [Pg.258]    [Pg.260]    [Pg.262]    [Pg.264]    [Pg.266]    [Pg.268]    [Pg.270]    [Pg.272]    [Pg.274]    [Pg.237]    [Pg.238]    [Pg.240]    [Pg.242]    [Pg.244]    [Pg.246]    [Pg.248]    [Pg.250]    [Pg.252]    [Pg.254]    [Pg.256]    [Pg.258]    [Pg.260]    [Pg.262]    [Pg.264]    [Pg.266]    [Pg.268]    [Pg.270]    [Pg.272]    [Pg.274]    [Pg.42]    [Pg.115]    [Pg.128]    [Pg.137]    [Pg.215]    [Pg.237]    [Pg.253]    [Pg.255]    [Pg.257]    [Pg.259]    [Pg.261]    [Pg.262]    [Pg.265]    [Pg.267]    [Pg.269]    [Pg.271]    [Pg.273]    [Pg.225]    [Pg.9]    [Pg.84]    [Pg.23]    [Pg.138]    [Pg.7]    [Pg.139]    [Pg.160]   


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Oversight

Vigil

Vigilant

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